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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062293Generated: October 31, 2026

Trifluoroacetic acid → 2-(4-(4-Aminopiperidin-1-yl)quinazolin-2-yl)phenol

https://huagongshe.com/reaction/2062293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 1-(2-(2-hydroxyphenyl)quinazolin-4-yl)piperidin-4-ylcarbamateHCID 136121521—
SolventDichloromethaneHCID 6344—
Product2-(4-(4-Aminopiperidin-1-yl)quinazolin-2-yl)phenolHCID 13612140684%

Reaction Steps

To a solution of tert-butyl 1-(2-(2-hydroxyphenyl)quinazolin-4-yl)piperidin-4-ylcarbamate (3.27 g, 8.09 mmol) in CH2Cl2 (75 mL) was added TFA (50 mL). The reaction was complete after 45 minutes After evaporating the solvents in vacuo, the crude material was diluted with CH2Cl2 and neutralized by adding a 1 N aqueous NaOH solution. The layers were separated, and the aqueous layer was extracted with CH2Cl2 (2×15 mL). The combined organic layers were dried over MgSO4, filtered, and concentrated to afford 2-(4-(4-aminopiperidin-1-yl)quinazolin-2-yl)phenol as a solid (2.09 g, 84%). LC/MS: m/z 321.3 (M+H)+ at 1.28 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA))

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283354B2
Source datasetuspto-grants-2012_10
ORD IDord-293e93075d1544199fcdda4f52df723e
Source noteuspto-grants-2012_10