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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711024Generated: November 1, 2026

4-Chloro-6-(phenylethynyl)pyrimidin-5-amine → 4-Chloro-6-phenyl-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1711024

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-(phenylethynyl)pyrimidin-5-amineHCID 59424578—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-Chloro-6-phenyl-5H-pyrrolo[3,2-d]pyrimidineHCID 57355036—

Reaction Steps

To a solution of 251 (30.8 mg, 0.134 mmol) in NMP (1.4 mL) a suspension of KH in mineral oil (35%, 31 mL, 0.268 mmol) was added in one portion. The mixture was stirred at room temperature overnight and partitioned between EtOAc and water. The organic phase was collected, dried over anhydrous Na2SO4 and concentrated. The residue was purified by flash chromatography, eluent EtOAc/hexane (1:2) to afford title compound affording 252 (22.7 mg, 74% yield). MS (m/z): 230.1 (100%) 232.1 (33%) (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790729B2
Source datasetuspto-grants-2010_09
ORD IDord-5c6928c172254802833c6f417e9a0e64
Source noteuspto-grants-2010_09