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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336992Generated: October 28, 2026

4-Aminobenzamide → HCID 71468816, compound

https://huagongshe.com/reaction/336992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzamideHCID 76079—
ReactantHCID 71471704HCID 71471704—
SolventPyridineHCID 1049—
ProductHCID 71468816HCID 7146881662%

Reaction Steps

Stir a mixture of 3-(5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carbonyl chloride (48 mg, 0.1 mmol) and 4-aminobenzamide (27 mg, 0.2 mmo) in pyridine (3 mL) at ambient temperature overnight. After removal solvent under vacuum, purify the residue by preparative HPLC to afford N-(4-carbamoylphenyl)-3-(5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxamide as a white solid (36 mg, 62.0%). MS (m/z): 582.1 (M+1). 1H NMR (CDCl3, 400 MHz) δ 7.84 (d, J=8.4 Hz, 2H), 7.65-7.63 (m, 3H), 7.49 (s, 2H), 7.44 (s, 1H), 6.03 (s, 1H), 5.61 (s, 1H), 4.09-4.05 (d, J=16 Hz, 1H), 3.72-3.68 (d, J=16 Hz, 1H), 3.07 (s, 2H), 2.94 (s, 2H), 1.76 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889710B2
Source datasetuspto-grants-2014_11
ORD IDord-f271d5d35905440e8fdd1b0d9ba0eafc
Source noteuspto-grants-2014_11