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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845789Generated: November 1, 2026

2-Chloropyrimidine → HCID 13588090, compound

https://huagongshe.com/reaction/845789

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyrimidineHCID 74404—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[1-(2-aminoethyl)-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amineHCID 12891741—
SolventEthanolHCID 702—
ProductHCID 13588090HCID 1358809061%

Reaction Steps

A mixture of 34.5 parts of 2-chloropyrimidine, 110 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-amine, 25 parts of sodium hydrogen carbonate and 1200 parts of ethanol was stirred and refluxed overnight. The reaction mixture was cooled and filtered over Hyflo. The filtrate was evaporated. The residue was purified by HPLC over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) saturated with ammonia, as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile, yielding 82 parts (61%) of 1-[(4-fluorophenyl)methyl]-N-[1-[2-[(2-pyrimidinyl)amino]-ethyl]-4-piperidinyl]-1H-benzimidazol-2-amine; mp. 168.4° C. (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04760074
Source datasetuspto-grants-1988_07
ORD IDord-ce32b63f03cd4f21a0d7e9070962291f
Source noteuspto-grants-1988_07