HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370136Generated: October 31, 2026
Methyl Isocyanate → HCID 178485942, compound
https://huagongshe.com/reaction/1370136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178490877 | HCID 178490877 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178485942 | HCID 178485942 | 60.6% |
Reaction Steps
A mixture of 1-(trans-4-aminocyclohexyl)-3-(3-chloro-4-methoxybenzyl)-5-cyano-2,3-dihydro-1H-benzimidazol-2-one (100 mg) and methyl isocyanate (17 mg) in dichloromethane (3 mL) was stirred at 0° C. for 2 hours under nitrogen atmosphere. The mixture was partitioned between water and a mixture of chloroform and methanol (5:1). The separated organic layer was washed with water and dried over magnesium sulfate. After evaporation of the solvent, the residue was subjected to a preparative thin-layer chromatography eluting with a mixture of chloroform and methanol (10:1). The obtained substance was triturated with diethyl ether to give 3-(3-chloro-4-methoxybenzyl)-5-cyano-1-[trans-4-(3-methylureido)cyclohexyl]-2,3-dihydro-1H-benzimidazol-2-one (69 mg) as colorless powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06582351B1 |
|---|
| Source dataset | uspto-grants-2003_06 |
|---|
| ORD ID | ord-ce269b92319a4c81a1124e9f020bc7e4 |
|---|
| Source note | uspto-grants-2003_06 |
|---|