HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 18680910, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 18681159 | HCID 18681159 | — |
| Catalyst | Dichloromethane | HCID 6344 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18680910 | HCID 18680910 | — |
Reaction Steps
Oxalyl chloride (0.208 ml) was added dropwise to a suspension prepared by adding 390 mg of 6-carboxy-1-(2-chlorobenzyl)-2-cyclopropylbenzimidazole to 10 ml of methylene chloride containing 1 drop of N,N-dimethylformamide at room temperature over a period of several minutes. The mixture was stirred at the same temperature for 2 hours, and was then concentrated under reduced pressure. Isopropyl ether was added to the residue, and the mixture was pulverized to give 450 mg of 1-(2-chlorobenzyl)-6-chlorocarbonyl-2-cyclopropylbenzimidazole hydrochloride (60) as a white powder. Since this product was unstable, it was used as a starting material in the subsequent step without being purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352985B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-a2ba4306d8044ec5b620c73916a02a7d |
| Source note | uspto-grants-2002_03 |