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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572322Generated: October 31, 2026

5-(4-Methyl-5-trifluoromethyl-isoxazol-3-yl)-thiophene-2-carboxylic acid → HCID 57606126, compound

https://huagongshe.com/reaction/572322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Methyl-5-trifluoromethyl-isoxazol-3-yl)-thiophene-2-carboxylic acidHCID 25210997—
Reactant3-(Trifluoromethyl)piperidine hydrochlorideHCID 68566404—
ProductHCID 57606126HCID 57606126—

Reaction Steps

Prepared from 5-(5-Trifluoromethyl-4-methyl-isoxazol-3-yl)-thiophene-2-carboxylic acid and (±)-3-trifluoromethylpiperidine hydrochloride by the method described in Example 41. Colorless solid (123 mg, 82%). 1H NMR (CDCl3) 1.53-1.76 (m, br, 2H), 1.84-1.95 (m, br, 1H), 2.10-2.22 (m, br, 1H), 2.31-2.43 (m, br, 4H), 2.92-3.16 (m, br, 2H), 4.28-4.45 (m, br, 1H), 4.54-4.72 (m, br, 1H), 7.34 (d, J=4.0, 1H), 7.47 (d, J=4.0, 1H). 13C NMR 7.7, 23.5, 24.2, 40.5 (q, J=27), 44.0 (br), 46.3 (br), 114.5 (q, J=2), 118.5 (q, J=271), 126.1 (q, J=283), 127.8, 129.1, 131.4, 139.3, 155.0 (q, J=41), 157.6, 162.8. 19F NMR −72.8, −63.2. LC/MS 6.99 min, [M+1]+ 413.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029397B2
Source datasetuspto-grants-2015_05
ORD IDord-47e7375dfe0e4449b8db8a34af8a9407
Source noteuspto-grants-2015_05