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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280353Generated: October 30, 2026

Acetic Anhydride → HCID 13653889, compound

https://huagongshe.com/reaction/280353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 13983254HCID 13983254—
SolventWaterHCID 962—
ProductHCID 13653889HCID 13653889—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588722
Source datasetuspto-grants-1986_05
ORD IDord-eb4c05ca694440399352fccfd29c29ee
Source noteuspto-grants-1986_05