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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062310Generated: November 2, 2026

Trifluoroacetic acid → (R)-2-(4-(3-aminopyrrolidin-1-yl)-7-methylquinazolin-2-yl)phenol

https://huagongshe.com/reaction/2062310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl(R)-1-(2-(2-hydroxyphenyl)-7-methylquinazolin-4-yl)pyrrolidin-3-ylcarbamateHCID 136121326—
SolventDichloromethaneHCID 6344—
Product(R)-2-(4-(3-aminopyrrolidin-1-yl)-7-methylquinazolin-2-yl)phenolHCID 136121376—

Reaction Steps

To 850 mg (2.02 mmol) of (R)-{1-[2-(2-hydroxy-phenyl)-7-methyl-quinazolin-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester was added at room temperature 4 mL of 1:1 TFA: CH2Cl2. The reaction mixture was stirred for 50 min and diluted with 20 mL of CH2Cl2 and extracted with 15 mL of satd. NaHCO3 solution. The organic layer was separated and dried over Na2SO4, and the solvent was removed under reduced pressure to give (R)-2-[4-(3-amino-pyrrolidin-1-yl)-7-methyl-quinazolin-2-yl]-phenol as an oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283354B2
Source datasetuspto-grants-2012_10
ORD IDord-15f2cf1c675e4a1687798893aaa6f87c
Source noteuspto-grants-2012_10