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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365765Generated: October 30, 2026

3-(Trifluoromethyl)benzoyl chloride → HCID 45381102, compound

https://huagongshe.com/reaction/2365765

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
ReactantHCID 58506741HCID 58506741—
SolventDichloromethaneHCID 6344—
ProductHCID 45381102HCID 45381102—

Reaction Steps

A solution of 3-(4-aminophenyl)-1-((S)-tetrahydrofuran-3-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.1 g, 0.34 mmol) in CH2Cl2 (10 mL) was cooled in an ice-water bath. To this, 3-(trifluoromethyl)benzoyl chloride (0.050 mL, 0.34 mmol) diluted in CH2Cl2 (5 mL) was added dropwise. The reaction was allowed to warm to room temperature and left stirring for 12 hours. The reaction proceeded until completion as judged by TLC and LC-MS, was concentrated in vacuo, resuspended in 50:50 H2O—CH3CN, and purified on a C18 column in CH3CN/H2O/0.1% TFA (1-100% gradient) to afford AD67. ESI-MS m/z [M+H]+ found 469.4, calculated 469.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697709B2
Source datasetuspto-grants-2014_04
ORD IDord-80b7b952e2f746efb63f339353d90c24
Source noteuspto-grants-2014_04