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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620156Generated: October 30, 2026

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

https://huagongshe.com/reaction/620156

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-piperidinopyrimidine (2.89 g) and 2-mercapto-5-methoxybenzimidazole (2.46 g) in ethanol (40 ml) and lN 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 numberUS04820708
Source datasetuspto-grants-1989_04
ORD IDord-c57b2c3864d04b71895a08da403b1409
Source noteuspto-grants-1989_04