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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227951Generated: October 30, 2026

Acetic Acid → HCID 18753460, compound

https://huagongshe.com/reaction/2227951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopentylamineHCID 2906—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22478201HCID 22478201—
SolventWaterHCID 962—
ProductHCID 18753460HCID 1875346036%

Reaction Steps

A mixture of 4-(4-chloro-2-fluoroanilino)-7-(2,2-dimethoxyethoxy)-6-methoxyquinazoline (210 mg, 0.52 mmol), water (5 ml) and TFA (5 ml) was stirred at ambient temperature for 3 hours then heated at 60° C. for 1 hour. The solution was allowed to cool, then diluted with water and the resulting precipitate was collected by filtration and dried. The solid was dissolved in methanol (10 ml) and cyclopentylamine (0.057 ml, 0.57 mmol) and dried 3 Å molecular sieves (2.5g) were added. The mixture was stirred for 30 minutes, glacial acetic acid (0.20 ml, 3.2 mmol) and sodium cyanoborohydride (150 mg, 2.4 mmol) were added and the reaction stirred for 4 hours then left to stand for 18 homs. The insolubles were removed by filtration and the solvent was removed from the filtrate by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol/aqueous ammonia (1008/1). The purified product was triturated with ether/hexane, collected by filtration and dried to give 4-(4-chloro-2-fluoroanilino)-7-(2-cyclopentylaminoethoxy)-6-methoxyquinazoline (80 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414148B1
Source datasetuspto-grants-2002_07
ORD IDord-9111bd91f02249d5a4a7396d47cb439b
Source noteuspto-grants-2002_07