HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280353Generated: October 30, 2026
Acetic Anhydride → HCID 13653889, compound
https://huagongshe.com/reaction/280353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 13983254 | HCID 13983254 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13653889 | HCID 13653889 | — |
Reaction Steps
A mixture of 7.7 parts of 2-amino-N-[2-[4-[[1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]benzamide, 20 parts of acetic acid anhydride and 80 parts of water was stirred for 4 hours at 100° C. Water was added and the whole was alkalized with ammonium hydroxide. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized from 4-methyl-2-pentanone. The product was filtered off and recrystallized from acetonitrile, yielding 7.7 parts of 2-(acetylamino)-N-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]benzamide; mp. 170.9° C. (compound 51).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04588722 |
|---|
| Source dataset | uspto-grants-1986_05 |
|---|
| ORD ID | ord-eb4c05ca694440399352fccfd29c29ee |
|---|
| Source note | uspto-grants-1986_05 |
|---|