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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908936Generated: November 2, 2026

2-(Trifluoromethyl)benzoyl chloride → propyl 2-{[2-(trifluoromethyl)benzoyl]amino}-5,6,7,8-tetrahydro-4H-5,8-epoxycyclohepta[b]thiophene-3-carboxylate

https://huagongshe.com/reaction/1908936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
Reactantpropyl 2-amino-5,6,7,8-tetrahydro-4H-5,8-epoxycyclohepta[b]thiophene-3-carboxylateHCID 66846079—
Productpropyl 2-{[2-(trifluoromethyl)benzoyl]amino}-5,6,7,8-tetrahydro-4H-5,8-epoxycyclohepta[b]thiophene-3-carboxylateHCID 25003090—

Reaction Steps

The title compound was prepared from the product of Example 34A and commercially available 2-trifluoromethyl-benzoyl chloride according to the procedure described for Example 1C. 1H NMR (DMSO-d6, 300 MHz) δ 0.92 (t, J=7.5 Hz, 3H), 1.64-1.71 (m, 3H), 1.98-2.15 (m, 3H), 2.58 (d, J=17.0 Hz, 1H), 3.11 (dd, J=16.6, 4.4 Hz, 1H), 4.16 (t, J=6.4 Hz, 2H), 4.69-4.74 (m, 1H), 5.14-5.16 (m, 1H), 7.80-7.94 (m, 4H), 11.40 (br s, 1H); MS (ESI+) m/z 440 (M+H)+. Anal. calcd. for C21H20F3NO4S: C, 57.40; H, 4.59; N, 3.19. Found: C, 57.44; H, 4.47; N, 3.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598224B2
Source datasetuspto-grants-2013_12
ORD IDord-48ba24963b414cb2a5198d32ac857d37
Source noteuspto-grants-2013_12