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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637421Generated: October 29, 2026

2-Chloropyrimidine → HCID 13588114, compound

https://huagongshe.com/reaction/637421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyrimidineHCID 74404—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13588089HCID 13588089—
SolventEthanolHCID 702—
ProductHCID 13588114HCID 1358811483%

Reaction Steps

A mixture of 1.7 parts of 2-chloropyrimidine, 9.66 parts of 2-[[1-(2-aminoethyl)-4-piperidinyl]amino]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-5-ol trihydrobromide, 5 parts of sodium hydrogen carbonate and 80 parts of ethanol was stirred and refluxed overnight. The reaction mixture was evaporated and the residue was taken up in trichloromethane. The organic phase was washed with water, dried, filtered and evaporated. The residue was crystallized from a mixture of acetonitrile and methanol, yielding 5.2 parts (83%) of 1-[(4-fluorophenyl)methyl]-2-[[1-[2-(2-pyrimidinylamino)ethyl]-4-piperidinyl]amino]-1H-benzimidazol-5-ol; mp. 194.4° C. (compound 64).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556660
Source datasetuspto-grants-1985_12
ORD IDord-4ca5523f348b43c38c725c4704a988aa
Source noteuspto-grants-1985_12