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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079373Generated: November 3, 2026

Trifluoroacetic acid → HCID 136104957, compound

https://huagongshe.com/reaction/2079373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 136121342HCID 136121342—
SolventDichloromethaneHCID 6344—
ProductHCID 136104957HCID 13610495783.4%

Reaction Steps

tert-Butyl 1-(2-(2-hydroxyphenyl)-7-methylquinazolin-4-yl)piperidin-4-ylcarbamate (3.21 g, 7.39 mmol) was dissolved in CH2Cl2 (55 ml). TFA (50 ml) was added and the reaction was stirred for 1 hour. After evaporating the solvents in vacuo, the crude material was diluted with CH2Cl2 and neutralized with a 1 N NaOH solution. The layers were separated, and the aqueous layer was extracted three times with CH2Cl2 (30 ml). The combined organic layers were dried over MgSO4, filtered, and concentrated to give 2-(4-(4-aminopiperidin-1-yl)-7-methylquinazolin-2-yl)phenol as a yellow solid (2.06 g, 83%). LC/MS: m/z 335.3 (M+H)+ at 1.42 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-2027641e7c224a2eab53541637431696
Source noteuspto-grants-2011_04