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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867718Generated: October 31, 2026

Sodium borohydride → {4-[(3-Chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methanol

https://huagongshe.com/reaction/1867718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-[(3-Chloro-2-fluorophenyl)amino]-7-methoxyquinazoline-6-carbaldehydeHCID 11573492—
SolventMethanolHCID 887—
Product{4-[(3-Chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methanolHCID 57979865100%

Reaction Steps

Sodium borohydride (0.046 g, 1.21 mmol) was added to a stirred suspension of 4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazoline-6-carbaldehyde (0.20 g, 0.604 mmol) in methanol (1 ml) at 0° C., over period of 5 minutes. The reaction mixture was allowed to stir at room temperature for 10 minutes and concentrated to dryness. The resulting grey solid was washed with water (2×1 ml) and dried to a constant weight under high vacuum at 40° C. to afford {4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methanol (0.2 g, 100%) as a grey solid; Mass Spectrum: (M+H)+ 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632840B2
Source datasetuspto-grants-2009_12
ORD IDord-6568c008c0534ba5829e75d4e95908cc
Source noteuspto-grants-2009_12