HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699619Generated: November 2, 2026
Ammonia → 6-Carbamoyl-1-(2,4-dichlorobenzyl)-2-methylbenzimidazole
https://huagongshe.com/reaction/1699619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Chloride | HCID 312 | — |
| Reactant | 1-(2,4-Dichlorobenzyl)-2-methyl-1H-benzo[d]imidazole-6-carboxylic acid | HCID 22508821 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Carbamoyl-1-(2,4-dichlorobenzyl)-2-methylbenzimidazole | HCID 18681118 | — |
Reaction Steps
Oxylyl chloride (0.437 g) is added to a methylene chloride (8 ml) solution of 6-carboxy-1-(2,4-dichlorobenzyl)-2-methylbenzimidazole (0.490 g) and N,N-dimethylformamide (1 drop) under ice-chilled conditions, and the solution is stirred for 1.5 hours at room temperature. Then, 28% aqueous ammonia (4 ml) is added and the solution is stirred for 12 hours at room temperature. Water and methylene chloride are added to the reaction solution for extraction. After the organic layer is concentrated, precipitated crystals are collected, dried and 6-carbamoyl-1-(2,4-dichlorobenzyl)-2-methylbenzimidazole (0.240 g) is obtained. 1H-NMR (DMSO-d6, δ): 2.48 (3H, s), 5.54 (2H, s), 6.41 (1H, d, J=8.4 Hz), 7.21-8.02 (3H, m), 7.31 (1H, dd, J=2.2 and 8.4 Hz), 7.60 (1H, d, J=8.4 Hz), 7.75 (1H, m), 7.93 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06348032B1 |
|---|
| Source dataset | uspto-grants-2002_02 |
|---|
| ORD ID | ord-ac6e3d888c8c449bb604348bde1839de |
|---|
| Source note | uspto-grants-2002_02 |
|---|