Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867878Generated: November 1, 2026

2-(Chloromethyl)-4-(piperidin-1-yl)pyrimidine → HCID 178488127, compound

https://huagongshe.com/reaction/867878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Chloromethyl)-4-(piperidin-1-yl)pyrimidineHCID 14306133—
ReactantHCID 178488032HCID 178488032—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
ProductHCID 178488127HCID 17848812772.1%

Reaction Steps

A mixture of 2-chloromethyl-4-piperidino-pyrimidine (2.89 g) and 2-mercapto-5-methoxybenzimidazole (2.46 g) in ethanol (40 ml) and 1N sodium hydroxide (15 ml) was stirred at room temperature for 16 hours. After stripping the residue was washed with water and recrystallised from acetonitrile to give 5-methoxy-2-(4-piperidino-2-pyrimidinylmethylthio)-(1H)-benzimidazole (3.5 g) m.p. 145°-147°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777172
Source datasetuspto-grants-1988_10
ORD IDord-fa4ff782cb5542498c78e9069a85370d
Source noteuspto-grants-1988_10