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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637427Generated: November 1, 2026

Acetic Acid → HCID 86740524, compound

https://huagongshe.com/reaction/637427

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 numberUS04556660
Source datasetuspto-grants-1985_12
ORD IDord-10ae4884ce62459ba6fbfba852cd07ef
Source noteuspto-grants-1985_12