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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884786Generated: October 31, 2026

Trifluoroacetic acid → 3-[5-Amino-4-benzoyl-3-(piperidin-4-yloxy)-pyrazol-1-yl]-n-cyclopropyl-4-methyl-benzamide, trifluoroacetate salt

https://huagongshe.com/reaction/884786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-[5-amino-4-benzoyl-1-(5-cyclopropylcarbamoyl-2-methyl-phenyl)-1H-pyrazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 11157237—
SolventDichloromethaneHCID 6344—
Product3-[5-Amino-4-benzoyl-3-(piperidin-4-yloxy)-pyrazol-1-yl]-n-cyclopropyl-4-methyl-benzamide, trifluoroacetate saltHCID 1127313259%

Reaction Steps

To a solution of 4-[5-amino-4-benzoyl-1-(5-cyclopropylcarbamoyl-2-methyl-phenyl)-1H-pyrazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl ester 8 (5.0 mg, 0.0089 mmol) in dichloromethane (2.0 ml) was added trifluoroacetic acid (0.5 ml). The mixture was stirred at room temperature for 3 h. Volatiles were removed in vacuo and the residue was washed with ether and a small amount of EtOAc to give the desired 3-[5-amino-4-benzoyl-3-(piperidin-4-yloxy)-pyrazol-1-yl]-N-cyclopropyl-4-methyl-benzamide, trifluoroacetate salt 9 as a white solid (3.0 mg, 59%). HPLC (4 minute 10-90 gradient) tR 1.75 min; MS m/z 460.1 [M+H]+; 1H NMR (DMSO-d6, 300 MHz) δ 8.50 (d, J=4.0, 1 H), 8.33 (bs, 2 H), 7.90 (d, J=8.0, 1 H), 7.83 (s, 1 H), 7.62 (d, J=7.0, 2 H), 7.44-7.52 (m, 4 H), 7.03 (bs, 2 H), 4.82 (m, 1 H), 2.97 (m, 2 H), 2.85 (m, 1 H), 2.73 (m, 2 H), 2.27 (s, 3 H), 1.91 (m, 2 H), 1.73 (m, 2 H), 0.71 (m, 2 H), 0.57 (m, 2 H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242117B2
Source datasetuspto-grants-2012_08
ORD IDord-9b9c5232cafd4b21af2fbb04651d8adb
Source noteuspto-grants-2012_08