HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21428970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 21428835 | HCID 21428835 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21428970 | HCID 21428970 | — |
Reaction Steps
A mixture of 1 part of 2-amino-N-{2-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]ethyl}-4-fluorobenzamide, 1 part of acetic acid anhydride and 15 parts of water is stirred for 30 minutes in a water-bath at 80°-90° C. The reaction mixture is cooled and alkalized with an ammonium hydroxide solution. The product is extracted with trichloromethane. The extract is dried, filtered and evaporated. The residue is crystallized from 4-methyl-2-pentanone. The product is filtered off and dried, yielding 0.5 parts of 2-(acetylamino)-N-{2-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]ethyl}-4-fluorobenzamide; mp. 210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04031226 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-eb0cc4983fda4398a59a46905d8eebba |
| Source note | uspto-grants-1977_06 |