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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244085Generated: October 25, 2026

Cyclopropylamine → N-cyclopropyl-7-fluoroquinazolin-4-amine

https://huagongshe.com/reaction/2244085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
Reactant4-Chloro-7-fluoroquinazolineHCID 16227013—
SolventDichloromethaneHCID 6344—
ProductN-cyclopropyl-7-fluoroquinazolin-4-amineHCID 2505969780%

Reaction Steps

4-Chloro-7-fluoro-quinazoline (0.73 g, 4 mmol) and cyclopropylamine (0.23 g, 4 mmol) are stirred in dichloromethane at ambient temperature overnight. The solid product is precipitated with hexanes, filtered, and washed with hexane and ethyl acetate, affording 0.3 g of desired Cyclopropyl-(7-fluoro-quinazolin-4-yl)-amine. The filtrate is concentrated and precipitated with hexanes, yielding an additional 0.35, for a combined yield of 80%. LC/MS m/z=204 [M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678803B2
Source datasetuspto-grants-2010_03
ORD IDord-d3116dd597eb4c88bb4beaff3f2791ad
Source noteuspto-grants-2010_03