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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803420Generated: November 2, 2026

Trifluoroacetic acid → Methyl-(2-pyridin-3-yl-4-trifluoromethyl-thiazol-5-yl)-amine

https://huagongshe.com/reaction/1803420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl-(2-pyridin-3-yl-4-trifluoromethyl-thiazol-5-yl)carbamic acid tert-butyl esterHCID 66645247—
Solvent1,2-DichloroethaneHCID 11—
ProductMethyl-(2-pyridin-3-yl-4-trifluoromethyl-thiazol-5-yl)-amineHCID 5958072381%

Reaction Steps

To a solution of DCE (4 mL) was added methyl-(2-pyridin-3-yl-4-trifluoromethyl-thiazol-5-yl)-carbamic acid tert-butyl ester (0.616 g, 1.7 mmol) and trifluoroacetic acid (4 mL) and the mixture was stirred for 15 min. The solvents were removed under reduced pressure and the resulting residue was re-dissolved in DCE and aqueous saturated NaHCO3. The biphasic mixture was separated and the aqueous layer was extracted three times with DCE. The organic extracts were combined, dried over MgSO4, filtered and concentrated to dryness under reduced pressure. The crude product was purified by silica gel column chromatography (0 to 100% ethyl acetate/hexanes) to give the desired product as an off-white solid (0.357 g, 80%): mp 152-157° C.; 1H NMR (300 MHz, CDCl3) δ 8.95 (d, J=2.3 Hz, 1H), 8.57 (dd, J=4.9, 1.7 Hz, 1H), 8.11 (dt, J=8.2, 2.3 Hz, 1H), 7.23 (ddd, J=7.9, 4.9, 0.7 Hz, 1H), 4.83 (br s, 1H), 3.05 (d, J=4.9 Hz, 3H); ESIMS m/z 260 (M+1), m/z 257.9 (M-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350044B2
Source datasetuspto-grants-2013_01
ORD IDord-ed0de40ec7464969acf79a616c5c37b8
Source noteuspto-grants-2013_01