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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793415Generated: November 2, 2026

tert-Butyl (4-aminophenyl)carbamate → HCID 22022165, compound

https://huagongshe.com/reaction/1793415

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (4-aminophenyl)carbamateHCID 688611—
Reactant4-Chloro-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolineHCID 11823941—
SolventIsopropanolHCID 3776—
ProductHCID 22022165HCID 22022165189.4%

Reaction Steps

A solution of N-(t-butoxycarbonyl) 4-aminoaniline (5.73 g, 27.5 mmol), and 4-chloro-6-methoxy-7-(3-morpholinopropoxy)quinazoline (8.44 g, 25.0 mmol), in isopropanol (100 ml) was heated at reflux for 3.5 hours before the reaction was allowed to cool to ambient temperature. The solid which had precipitated was collected by suction filtration and washed with diethyl ether (2×100 ml). Drying of this material yielded 4-(4-(N-Boc-amino)anilino)-6-methoxy-7-(3-morpholinopropoxy)quinazoline dihydrochloride (13.79 g, 95% yield) as a white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081461B1
Source datasetuspto-grants-2006_07
ORD IDord-40883f32ac2e49d894bc6c508a078743
Source noteuspto-grants-2006_07