Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410617Generated: November 1, 2026

Trifluoroacetic acid → HCID 58456358, compound

https://huagongshe.com/reaction/410617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58456281HCID 58456281—
SolventDichloromethaneHCID 6344—
ProductHCID 58456358HCID 58456358127.2%

Reaction Steps

tert-Butyl 1-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]cyclopropanecarboxylate (375 mg, 0.787 mmol) was taken up in CH2Cl2 (12 mL) before adding TFA (3 mL). The reaction was stirred at room temperature overnight. The reaction was evaporated to dryness, and the residue was azeotroped with DCE (3×) to provide 1-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]cyclopropanecarboxylic acid (TFA salt) (421 mg, 100%) as a yellow solid. MS ESI: [M+H]+ m/z 421.0. 1H NMR (600 MHz, DMSO-d6) δ 13.15 (s, 1H), 10.21 (s, 1H), 8.80 (d, J=4.8, 1H), 7.95 (s, 1H), 7.87 (s, 1H), 7.44 (s, 1H), 7.25 (d, J=4.9, 1H), 7.12 (s, 1H), 2.29 (s, 3H), 1.81-1.62 (m, 4H). rhSYK activity=+++

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-512774319f8a4658bfdd1cbb4601a716
Source noteuspto-grants-2014_06