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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72708Generated: October 26, 2026

Azetidine → 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/72708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzetidineHCID 10422—
Reactant4,6-Dichloro-5-pyrimidinecarbaldehydeHCID 819691—
CatalystTriethylamineHCID 8471—
SolventChloroformHCID 6212—
Product4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehydeHCID 86712562—

Reaction Steps

To a solution of 4,6-dichloropyrimidine-5-carbaldehyde (1.00 g, 5.65 mmol) in chloroform at 0° C. were added azetidine (99%, 0.392 mL, 5.71 mmol) and triethylamine (5 drops). The reaction mixture was allowed to warm to room temperature and then stirred for 18 hours. The reaction mixture was filtered, and the filtrate was purified by silica gel chromatography (Gradient: 0% to 100% ethyl acetate in heptane) to provide the product. Yield: 880 mg, 4.45 mmol, 79%. LCMS m/z 198.1, 200.1 (M+1). 1H NMR (400 MHz, CD3OD) δ 2.34-2.43 (m, 2H), 4.12-4.33 (br m, 4H), 8.30 (s, 1H), 10.28 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829010B2
Source datasetuspto-grants-2014_09
ORD IDord-50b2e28456f84a5494615235ad31a5bc
Source noteuspto-grants-2014_09