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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766087Generated: October 31, 2026

Potassium Carbonate → tert-Butyl 5-amino-2-methylthio-4-(3-(2-(pyrrolidin-1-yl)-ethoxy)-phenyl)-quinazoline-6-carboxamide

https://huagongshe.com/reaction/1766087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Chloroethyl)pyrrolidine hydrochlorideHCID 81668—
Reactanttert-Butyl 5-amino-2-methylthio-4-(3-hydroxyphenyl)-quinazoline-6-carboxamideHCID 21109116—
SolventAcetoneHCID 180—
Producttert-Butyl 5-amino-2-methylthio-4-(3-(2-(pyrrolidin-1-yl)-ethoxy)-phenyl)-quinazoline-6-carboxamideHCID 21109110—

Reaction Steps

A mixture of K2CO3 (1.0 g), 1-(2-chloroethyl)pyrrolidine hydrochloride (66 mg) and tert-butyl 5-amino-2-methylthio-4-(3-hydroxyphenyl)-quinazoline-6-carboxamide (example 26a, 121 mg) in acetone was heated overnight at reflux. The mixture was cooled to room temperature, the solids were removed by filtration and the filtrate concentrated under reduced pressure. The residue was taken up in EtOAc and washed with water and brine. The organic phase was dried (MgSO4) and concentrated in vacuo. The title compound was purified by HPLC using a Luna C-18 column with the following gradient: 10% aq. CH3CN/CH3CN/0.1% aq. TFA=72/25/3 to 27/70/3 (v/v/v) in 30 min. The title compound was lyophilized from a nixture of water, TFA is and CH3CN.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229990B2
Source datasetuspto-grants-2007_06
ORD IDord-85f7e2ba71c345e9b66af5ae84d69418
Source noteuspto-grants-2007_06