Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534748Generated: November 2, 2026

Acetic Acid → HCID 86740524, compound

https://huagongshe.com/reaction/1534748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13588090HCID 13588090—
ProductHCID 86740524HCID 8674052416.5%

Reaction Steps

A mixture of 4.5 parts of 1-[(4-fluorophenyl)methyl]-N-[1-[2-[(2-pyrimidinyl)amino]ethyl]-4-piperidinyl]-1H-benzimidazol-2-amine, 15 parts of acetic acid anhydride and 140 parts of acetic acid was stirred and refluxed overnight. The reaction mixture was evaporated. The residue was taken up in water and the whole was alkalized with ammonium hydroxide. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by HPLC over silica gel using a mixture of methylbenzene and ethanol (90:10 by volume) as eluent. The second fraction was collected and the eluent was evaporated. The residue was converted into the (E)-2-butenedioate salt in methanol. The salt is filtered off and dried, yielding 1.2 parts (16.5%) of N-[2-[4-[[1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]-N-(2-pyrimidinyl)acetamide (E)-2-butenedioate (1:2); mp. 191.1° C. (compound 99).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE033833
Source datasetuspto-grants-1992_02
ORD IDord-2aab4c9ecf194794acaa84bdbc12704a
Source noteuspto-grants-1992_02