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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34759Generated: October 25, 2026

2-Chloroacrylonitrile → 4-Amino-2-(4-phthalimidobutyl)pyrimidine

https://huagongshe.com/reaction/34759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacrylonitrileHCID 70198—
Reactant1,5-Diazabicyclo(5,4,0)undec-5-eneHCID 314112—
Reactant1-Amidino-4-phthalimidobutane hydrochlorideHCID 21298870—
SolventAcetonitrileHCID 6342—
Product4-Amino-2-(4-phthalimidobutyl)pyrimidineHCID 2045033742.2%

Reaction Steps

A solution of 2-chloroacrylonitrile (1.75 g.) in acetronitrile (10 ml.) was added over 15 minutes to an ice-cooled mixture of 1-amidino-4-phthalimidobutane hydrochloride (5.64 g.), acetonitrile (50 ml.) and 1,5-diazabicyclo[5,4,0]undec-5-ene (6.08 g.). The mixture was stirred for a further two hours and then evaporated to dryness. The residue was treated with water (50 ml.) and the mixture extracted with ethyl acetate (2×50 ml.). The combined ethyl acetate extracts were extracted with N hydrochloric acid (3×30 ml.) and the combined aqueous extracts neutralised with sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate extracts were evaporated to dryness and the residue recrystallised from acetonitrile to give 4-amino-2-(4-phthalimidobutyl)pyrimidine (2.5 g.), m.p. 139°-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762932
Source datasetuspto-grants-1988_08
ORD IDord-440b1d3585c8494281a1602658ea97d9
Source noteuspto-grants-1988_08