Category: imidazoles-derivatives

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 1003-21-0, name is 5-Bromo-1-methyl-1H-imidazole, A new synthetic method of this compound is introduced below., Computed Properties of C4H5BrN2

Example No. 18: Preparation of Compound No. 18[0306] A solution of 2,8-dimethyl-2,3,4,5-tetrahydro- lH-pyrido[4,3-b]indole (0.4 g, 2 mmol), 5-bromo-l-methyl-lH-imidazole (0.644 g, 4 mmol), K3P04 (0.848 g, 4 mmol), Cul (38 mg, 0.2 mmol) and L-Proline (46 mg, 0.39 mmol) in dry DMF (6 mL) was stirred at 150 C for 16h. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford crude material, which was purified by reverse phase HPLC to yield 2,8-dimethyl-5-(3-methyl-3H- imidazol-4-yl)-2,3,4,5-tetrahydro-lH-pyrido[4,3-b]indole (15 mg). 1H NMR (HC1 salt, CD3OD) delta (ppm): 9.20 (s, IH), 8.0 (s, IH), 7.40 (s, IH), 7.20 (d, IH), 7.10 (d, IH), 4.76 (d, IH), 4.40 (d, . n . m, H , . , H , . s, H , . m, z s, 3H).

The synthetic route of 1003-21-0 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; MEDIVATION TECHNOLOGIES, INC.; PROTTER, Andrew, Asher; CHAKRAVARTY, Sarvajit; WO2012/112962; (2012); A1;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 75370-65-9, name is 4-Amino-1H-benzo[d]imidazol-2(3H)-one, A new synthetic method of this compound is introduced below., Recommanded Product: 4-Amino-1H-benzo[d]imidazol-2(3H)-one

To a solution of 4-tert-butylbenzylamine (2 mL, 1 1.36 mmol) in THF (30 mL) was added CDI (2.1 mol eq, 3.86g) and the mixture was heated at 70C overnight. The reaction mixture was evaporated, water was added and the aqueous phase was extracted with EtOAc (3×30 mL). The recombined organic phases were anhydrified over Na2SO4 and evaporated at reduced pressure (pale yellow oil, quantitative yield). The oil obtained (1.6g, 6.2 mmol)) was dissolved in DMF (25mL) and the bicyclic amine la was added (0.8 mol eq, 0.74g), then the mixture obtained was heated at 100C overnight. The solvent was removed at reduced pressure and the residue was purified by crystallization from MeOH to obtain the product as a white solid (0.54g, 1.59 mmol, 26% Yield).1HNMR (DMSO, 400 MHz) delta 1.26 (s, 9H), 4.28 (d, 2H, J=6), 6.34 (dd, 1H), 6.36 (t, 1H), 6.83-6.91 (m, 2H), 7.26 (d, 2H, J=8), 7.37 (d, 2H, J=8), 8.20 (s, 1H9, 9.89 (bs, 1H), 10.61 (bs, 1H). [M+1] 338.82 (C19H22N4O2 requires 338.40).

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; PHARMESTE S.R.L.; NAPOLETANO, Mauro; TREVISANI, Marcello; PAVANI, Maria Giovanna; FRUTTAROLO, Francesca; WO2011/120604; (2011); A1;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 89830-98-8, name is 5-Cyclopropyl-1H-imidazole, This compound has unique chemical properties. The synthetic route is as follows., COA of Formula: C6H8N2

Step 2: methyl 2-(4-cyclopropyl-1H-imidazol-1-yl)-5-oxo-4,5,7,8-tetrahydro-[1,4]diazepino[7,1-a]isoquinoline-9-carboxylate A solution of methyl 2,5-dioxo-2,3,4,5,7,8-hexahydro-[1,4]diazepino[7,1-a]isoquinoline-9-carboxylate (225 mg, 0.79 mmol) in DCE (20 mL) was treated with POCl3 (0.37 mL, 3.93 mmol) and the mixture was heated to 100° C. for 1 h. The mixture was then allowed to cool to RT, and then concentrated in vacuo, and dried azeotropically with toluene. The residue obtained was taken up in DCE (40 mL) and 4-cyclopropyl-1H-imidazole (261 mg, 2.41 mmol) were added. The mixture was heated to to 100° C. for 1 h and then allowed to cool to RT, diluted with DCM and washed with a saturated aq, solution of NaHCO3. The org. layer was dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (SiO2, AcOEt/MeOH 100:0 to 90:10) and crystallization in Et2O/petroleum ether gave the title compound (116 mg). UPLC-MS: MS 377.2 (M+H+); UPLC rt 0.88 min. 1H NMR (600 MHz, DMSO-d6): delta ppm 0.54-0.73 (m, 2H); 0.73-0.88 (m, 2H); 1.74-1.89 (m, 1H); 3.25 (br s, 2H); 3.67-3.82 (m, 2H); 3.88 (s, 3H); 4.25 (br s, 2H); 7.13 (s, 1H); 7.44 (s, 1H); 7.48-7.57 (m, 1H); 7.96 (d, J=7.65 Hz, 1H); 8.09 (s, 1H); 8.19 (d, J=7.91, 1H).

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 89830-98-8.

Reference:
Patent; NOVARTIS AG; BEHNKE, Dirk; CARCACHE, David; ERTL, Peter; KOLLER, Manuel; ORAIN, David; US2014/57902; (2014); A1;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Electric Literature of 33016-47-6, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 33016-47-6 name is 1-Trityl-1H-imidazole-4-carbaldehyde, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

(a) 1-triphenylmethyl-4-[(1-hydroxy-1-phenyl)methyl]-1H-imidazole Prepared by reacting 4-formyl-1-triphenylmethyl-1H-imidazole (melting point: 202-205 C.; prepared by oxidation of the corresponding 4-hydroxymethyl compound with manganese dioxide in dioxane) with phenylmagnesium bromide in dry THF. Yield: 94% of theory; Melting point: 187-191 C.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 1-Trityl-1H-imidazole-4-carbaldehyde, and friends who are interested can also refer to it.

Reference:
Patent; Boehringer Ingelheim Pharma KG; US6043254; (2000); A;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Related Products of 496-46-8, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 496-46-8, name is Tetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione, This compound has unique chemical properties. The synthetic route is as follows.

A mixture of the diether (compound 2.5) of dimethylglycoluril (1 g, 3.9 mmol), glycoluril (1. 1 g, 7.75 mmol) and LICL (250 mg) were ground together to give a fine powder. To this mixture was added 8 M HCL (10 mL) and the mixture stirred for 1 hr at ambient temperature, after which time all the solid material had dissolved. The mixture was then heat at 50C for 12 to 24 hr. After cooling the solvent was evacuated in vacuo. Re- crystallisation from combinations of methanol and dilute acid solutions gave the trimer (compound 2.4) 1.2 g as a pure compound.

The chemical industry reduces the impact on the environment during synthesis Tetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione. I believe this compound will play a more active role in future production and life.

Reference:
Patent; UNISEARCH LIMITED; WO2005/26168; (2005); A1;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 2963-77-1 as follows. Formula: C13H11N3

General procedure: A suspension of amine A1-A3 (1 mmol) in water is takenin a round bottomed flask; to this sulphonyl chloride(1 mmol) was added. This was stirred at room temperature while monitoring the reaction. The product was filtered,recrystallised using methanol-water and column purified.The structures were confirmed by 1H NMR, 13C NMR, IRand mass spectral analysis.

According to the analysis of related databases, 2963-77-1, the application of this compound in the production field has become more and more popular.

Reference:
Article; Vangala, Radhika; Sivan, Sree Kanth; Peddi, Saikiran Reddy; Manga, Vijjulatha; Journal of Computer-Aided Molecular Design; vol. 34; 1; (2020); p. 39 – 54;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 1003-21-0, name is 5-Bromo-1-methyl-1H-imidazole, A new synthetic method of this compound is introduced below., SDS of cas: 1003-21-0

Isopropylmagnesium chloride lithium chloride complex (1.3 M in tetrahydrofuran, 2.0 mL, 2.60 mmol) was added to an ice-water cooled solution of 5-bromo-1-methyl-1H-imidazole (444 mg, 2.76 mmol) in tetrahydrofuran (12 mL). The resulting white suspension was stirred for 5 minutes then the cooling bath was removed. After 10 minutes, the suspension was added dropwise by syringe to an ice-water cooled mixture of (3-(4-(1H-1,2,4-triazol-1-yl)benzyl)-4-chloro-2-methoxyquinolin-6-yl)(4-chlorophenyl)methanone (772 mg, 1.59 mmol, Intermediate 45, step e) and lanthanum(III) chloride bis(lithium chloride) complex solution (0.6 M in tetrahydrofuran, 5.25 mL, 3.16 mmol) in tetrahydrofuran (15 mL). After 20 minutes, saturated aqueous ammonium chloride solution was added (2 mL) then the cooling bath was removed. The mixture was diluted with water (25 mL) and ethyl acetate (50 mL). The layers were separated. The aqueous layer was extracted with ethyl acetate (25 mL). The organic layers were combined and the combined solution was dried with sodium sulfate. The dried solution was filtered and the filtrate was absorbed onto 6 g of silica gel for dry-load flash-column chromatography on silica gel eluting with 100% dichloromethane initially for 5 minutes, grading to 7% methanol-dichloromethane over 30 minutes to afford the titled compound as a white solid. 1H NMR (400 MHz, CDCl3) delta ppm 8.43 (s, 1H), 8.12 (d, J=2.1 Hz, 1H), 8.06 (s, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.58-7.50 (m, 3H), 7.41 (d, J=8.5 Hz, 2H), 7.36 (d, J=1.1 Hz, 1H), 7.31 (s, 4H), 6.38 (d, J=1.1 Hz, 1H), 4.33 (s, 2H), 4.12 (s, 1H), 4.08 (s, 3H), 3.38 (s, 3H); MS m/e 571.1 [M+H]+. (3-(4-(iH-i,2,4-triazol-i-yl)ben- zyl)-4-chloro-2-methoxyquinolin-6-yl)(4-chlorophenyl)(i – methyl-iH-imidazol-5-yl)methanol was purified by HPEC (Chiralpak IA column, 50 mmx2SO mm, ethanol with 0.2% triethylamine as eluent, 30 mE/minute, 254 nm wavelength) to give two enantiomers. The first eluting enantiomer was Example 648: ?H NMR (400 MHz, CDC13) oe ppm 8.43 (s, iH), 8.12 (d, J=2.i Hz, iH), 8.06 (s, iH), 7.78 (d, J=8.7 Hz, iH), 7.56-7.50 (m, 3H), 7.41 (d, J=8.5 Hz, 2H), 7.36 (d, J=i .1 Hz, iH), 7.31 (s, 4H), 6.38 (d, J=i.i Hz, iH), 4.33 (s, 2H), 4.08 (s, 3H), 3.38 (s, 3H); MS mle 571.1 [M+H]+ and the second eluting enantiomer was Example 64C: ?H NMR (400 MHz, CDC13) oeppm8.43 (s, iH), 8.12 (d, J=2.i Hz, iH), 8.06 (s, iH), 7.78 (d, J=8.7 Hz, iH), 7.58-7.49 (m, 3H), 7.41 (d, J=8.6 Hz, 2H), 7.35 (s, iH), 7.31 (s, 4H), 6.38 (s, iH), 4.33 (s, 2H), 4.21 (s, iH), 4.08 (s, 3H), 3.38 (s, 3H); MS mle 571.1 [M+H] +.

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; Janssen Pharmaceutica NV; Leonard, Kristi A.; Barbay, Kent; Edwards, James P.; Kreutter, Kevin D.; Kummer, David A.; Maharoof, Umar; Nishimura, Rachel; Urbanski, Maud; Venkatesan, Hariharan; Wang, Aihua; Wolin, Ronald L.; Woods, Craig R.; Pierce, Joan; Goldberg, Steven; Fourie, Anne; Xue, Xiaohua; US2014/107094; (2014); A1;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Reference of 7189-69-7, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 7189-69-7, name is 1,1′-Sulfonyldiimidazole, This compound has unique chemical properties. The synthetic route is as follows.

A 20-mL vial was charged with N-(4-methoxybenzyl)-2-methylpyrimidin-4-amine (prepared analogous to Intermediate A, pages 43-44 of WO2013122897, wherein l,2,4-thiadiazol-5-amine was replaced with 2-methylpyrimidin-4-amine and 2,4-dimethoxybenzaldehyde was replaced with 4-methoxybenzaldehyde) (864 mg, 4.36 mmol) then purged with nitrogen. 2-Methyltetrahydrofuran (10.0 mL) and a solution of lithium hexamethyldisilazide in THF (1.0 M, 4.27 mL, 4.27 mmol) were added via syringe to the stirred reaction mixture. The vial was sealed with a Teflon coated cap and the reaction was warmed to 90 C and stirred vigorously. After 2 h, the red reaction mixture was allowed to cool to ambient temperature. The reaction mixture was diluted with water (25 mL) and EtOAc (25 mL). The layers were separated and the aqueous layer extracted with additional EtOAc (2 x 25 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure and purified by flash column chromatography (100-g silica gel Biotage column, eluent: gradient, 20 to 80% 3:1 EtOAc/EtOH in heptane with DCM as a 10% additive) to afford N-(4-methoxybenzyl)-N-(2-methylpyrimidin-4-y 1)-1 H-imidazole-1 -sulfonamide (450 mg, 1.25 mmol, 57.4 % yield) asa light-yellow solid, m/z (ESI) 360.2 (M+H)+

The chemical industry reduces the impact on the environment during synthesis 1,1′-Sulfonyldiimidazole. I believe this compound will play a more active role in future production and life.

Reference:
Patent; USA Anjin Corporation; M .weisi; B .C.miergelamu; T .dining; J .siteerwogen; A .gusiman-peileisi; A .beiqiao; I .E.makesi; (177 pag.)CN107531705; (2018); A;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 934-32-7 as follows. COA of Formula: C7H7N3

General procedure: A mixture of 2-aminobenzimidazole (1, 1 mmol), 4-bromobenzaldehyde (2a, 1 mmol), malononitrile (3,1 mmol) and p-TSA (10 mol%) was stirred at 80 8C undersolvent-free conditions for 30 min (Table 3, entry 1). Theprogress of the reaction was monitored by TLC. Aftercompletion of the reaction, the reaction mixture waswashed with water and ethanol, and the residue recrystallizedfrom ethanol to afford the pure product 4a (92%).

According to the analysis of related databases, 934-32-7, the application of this compound in the production field has become more and more popular.

Reference:
Article; Reddy, Mudumala Veeranarayana; Oh, Jeongsu; Jeong, Yeon Tae; Comptes Rendus Chimie; vol. 17; 5; (2014); p. 484 – 489;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Adding a certain compound to certain chemical reactions, such as: 6160-65-2, name is 1,1′-Thiocarbonyldiimidazole, belongs to imidazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 6160-65-2, Computed Properties of C7H6N4S

To a solution of TCDI (3.87 g, 19.55 mmol, 2.0 equiv) and DMAP (0.60 g, 4.88 mmol, 0.5 equiv) in DCM (110 mL) was added a solution of 12 (2.06 g, 9.77 mmol, 1.0 equiv) in DCM (38 mL) at 0 C. After being stirred for 10 h at rt, the resulting mixture was quenched with saturated NH4Cl solution (50 mL). The layers were separated and the aqueous layer was extracted with DCM (3×50 mL). The organic layers were combined, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc 2:1) to furnish 11 (2.06 g, 84%) as a white powder. Colorless block-shaped crystals of 11 were obtained by slow evaporation of a petroleum ether/DCM solution after several days. Mp 185-186 C; IR (thin film): numax 2966, 2924, 1707, 1565 cm-1; 1H NMR (400 MHz, CDCl3): delta 4.48 (d, J=8.8 Hz, A of AB, 1H), 4.35 (d, J=8.8 Hz, B of AB, 1H), 2.95 (dd, J=13.2, 3.2 Hz, 1H), 2.60 (d, J=14.4 Hz, A? of A?B?, 1H), 2.55 (d, J=14.4 Hz, B? of A?B?, 1H), 2.51 (dd, J=16.2, 5.0 Hz, 1H), 2.28 (ddd, J=16.5, 11.6, 8.0 Hz, 1H), 2.16-2.11 (m, 1H), 1.87-1.81 (m, 1H), 1.69 (ddd, J=8.0, 8.0, 3.6 Hz, 1H), 1.54 (dddd, J=12.6, 12.6, 12.6, 5.4 Hz, 1H), 1.02-0.95 (m, 1H), 0.76 (ddd, J=7.2, 3.6, 3.6 Hz, 1H), 0.61 (s, 3H); 13C NMR (100 MHz, CDCl3): delta 208.8, 190.7, 94.3, 72.6, 63.1, 56.3, 39.9, 39.3, 28.2, 27.9, 19.2, 18.3, 12.5; HRMS (ESI): m/z calcd for C13H16O3SNa [M+Na]+ 275.0718, found 275.0710.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 1,1′-Thiocarbonyldiimidazole, and friends who are interested can also refer to it.

Reference:
Article; Yue, Guizhou; Yang, Li; Yuan, Changchun; Du, Biao; Liu, Bo; Tetrahedron; vol. 68; 47; (2012); p. 9624 – 9637,14;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem