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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079675Generated: October 26, 2026

3-Chloro-4-morpholinoaniline → Tert-butyl 4-(5-bromo-2-(3-chloro-4-morpholinophenylamino) quinazolin-8-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/2079675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-morpholinoanilineHCID 108661—
ReactantTert-butyl 4-(5-bromo-2-chloroquinazolin-8-yloxy)piperidine-1-carboxylateHCID 86639323—
SolventIsopropanolHCID 3776—
ProductTert-butyl 4-(5-bromo-2-(3-chloro-4-morpholinophenylamino) quinazolin-8-yloxy)piperidine-1-carboxylateHCID 59199220—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of tert-butyl 4-(5-bromo-2-chloroquinazolin-8-yloxy)piperidine-1-carboxylate (1 eq) and N-(4-amino-2-chlorophenyl) morpholine (1 eq) in isopropanol was heated in a sealed tube at 110° C. for overnight. The reaction mixture was concentrated and proceeds for next step. ES/MS m/z 618.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932262B2
Source datasetuspto-grants-2011_04
ORD IDord-c48f8f4b1d484188b67c311bd92e861e
Source noteuspto-grants-2011_04