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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874396Generated: October 29, 2026

3-(Trifluoromethyl)benzoyl chloride → HCID 45381324, compound

https://huagongshe.com/reaction/874396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
ReactantHCID 58506753HCID 58506753—
SolventDichloromethaneHCID 6344—
ProductHCID 45381324HCID 45381324—

Reaction Steps

A solution of (S)-tert-butyl 3-(4-amino-3-(4-aminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)pyrrolidine-1-carboxylate (0.075 g, 0.17 mmol) in CH2Cl2 (10 mL) was cooled in an ice-water bath. To this, 3-(trifluoromethyl)benzoyl chloride (0.025 mL, 0.17 mmol) diluted in CH2Cl2 (5 mL) was added dropwise. The reaction was allowed to warm to room temperature and left stirring for 4 hours, yielding the benzamide derivative (ESI-MS m/z [M+H]+ found 568.5, calculated 568.6). Boc-deprotection was completed through the addition of formic acid (5 mL) and concentrated HCl (0.5 mL) added dropwise directly to the reaction mixture. The reaction mixture was left stirring for 12 hours and then 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 AD70. ESI-MS m/z [M+H]+ found 468.5, calculated 468.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980899B2
Source datasetuspto-grants-2015_03
ORD IDord-706762909c62434a8fc894bac4b7692f
Source noteuspto-grants-2015_03