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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079245Generated: October 31, 2026

Trifluoroacetic acid → HCID 136121493, compound

https://huagongshe.com/reaction/2079245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 136121359HCID 136121359—
SolventDichloromethaneHCID 6344—
ProductHCID 136121493HCID 13612149392%

Reaction Steps

To a solution of (R)-tert-butyl 2-((benzyloxy)methyl)-4-(2-(2-hydroxyphenyl)-7-methylquinazolin-4-yl)piperazine-1-carboxylate (760 mg, 1.72 mmol) in 15 mL CH2Cl2 was added 10 mL of TFA. The reaction was stirred for 1 hour. TFA was removed under vacuum and the reaction was neutralized using a 1 M NaOH solution. The aqueous layer was extracted twice with CH2Cl2, dried over Na2SO4, filtered, and concentrated to obtain 2-(4-((R)-3-((benzyloxy)methyl)piperazin-1-yl)-7-methylquinazolin-2-yl)phenol (570 mg, 92%). This material was used in the next step without further purification. LC/MS: m/z 441.5 (M+H)+ at 2.44 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-a390c5b6e09b4e5fbffccb0b6989ceb0
Source noteuspto-grants-2011_04