HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761513Generated: October 29, 2026
Dimethylformamide → HCID 178502018, compound
https://huagongshe.com/reaction/1761513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | HCID 178419604 | HCID 178419604 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178502018 | HCID 178502018 | 34.2% |
Reaction Steps
A mixture of 9.18 parts of methyl [5-[bromo(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]carbamate monohydrobromide, 12.3 parts of 2-methyl-1H-imidazole and 56.4 parts of N,N-dimethylformamide was stirred for 17 hours at room temperature. The reaction mixture was diluted with 300 parts of water. The precipitated product was filtered off and dissolved in dichloromethane. The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane, methanol and methanol, saturated with ammonia, (90:5:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 27 parts of ethyl acetate. The product was filtered off, washed with 1,1'-oxybisethane and dried, yielding 2.6 parts (34.2%) of methyl [5-[(4-fluorophenyl)(2-methyl-1H-imidazol-1-yl)methyl]-1H-benzimidazol-2-yl]carbamate; mp. >300° C. (compound 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04826862 |
|---|
| Source dataset | uspto-grants-1989_05 |
|---|
| ORD ID | ord-0caadf18b61a4089954f0ab8e4567f4d |
|---|
| Source note | uspto-grants-1989_05 |
|---|