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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798833Generated: November 3, 2026

2-Chloro-5-fluoro-4-methylpyrimidine → 2-{2-[1-(5-Fluoro-4-methylpyrimidin-2-yl)piperidin-4-yl]cyclopropyl}ethanol

https://huagongshe.com/reaction/1798833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-fluoro-4-methylpyrimidineHCID 20778073—
ReactantCis tert-butyl 4-[2-(2-hydroxyethyl)cyclopropyl]piperidine-1-carboxylateHCID 66935269—
Product2-{2-[1-(5-Fluoro-4-methylpyrimidin-2-yl)piperidin-4-yl]cyclopropyl}ethanolHCID 58128560—

Reaction Conditions

Temperature90 °C

Reaction Steps

The titled compound was prepared from 2-chloro-5-fluoro-4-methylpyrimidine and rac cis-tert-Butyl-4-[-2-(2-hydroxyethyl)cyclopropyl]piperidine-1-carboxylate by a procedure analogous to example 6 step 2, with the exception of reaction temperature. The reaction was heated at 90° C. for 2 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343990B2
Source datasetuspto-grants-2013_01
ORD IDord-4495146233c249cabe34a17605046948
Source noteuspto-grants-2013_01