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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172333Generated: October 26, 2026

3-Chloro-n-{[trans-4-(2,4-dichlorophenyl)-5-nitrocyclohex-1-en-1-yl]methyl}-4-(methylsulfonyl)thiophene-2-carboxamide → n-{[trans-5-Amino-4-(2,4-dichlorophenyl)cyclohex-1-en-1-yl]methyl}-3-chloro-4-(methylsulfonyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/1172333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-n-{[trans-4-(2,4-dichlorophenyl)-5-nitrocyclohex-1-en-1-yl]methyl}-4-(methylsulfonyl)thiophene-2-carboxamideHCID 68771931—
CatalystZincHCID 23994—
SolventAcetic acid methanolHCID 10129899—
Productn-{[trans-5-Amino-4-(2,4-dichlorophenyl)cyclohex-1-en-1-yl]methyl}-3-chloro-4-(methylsulfonyl)thiophene-2-carboxamideHCID 6877038366%

Reaction Steps

To a solution of Example 12D (40 mg, 0.077 mmol) in mixture of methanol/acetic acid (0.5 mL/0.5 mL), Zn powder (50 mg, 0.77 mmol) was added at room temperature. The reaction mixture was stirred for thirty minutes, filtered, concentrated under reduced pressure, and purified by high pressure liquid chromotography (eluting with 0-70% acetonitrile/water and 0.1% trifluoroacetic acid) to provide the title compound (25 mg, 66%). 1H NMR (400 MHz, methanol-d4) δ ppm 8.45 (s, 1H), 8.03 (s, 1H), 7.54 (s, 1H), 7.35-7.47 (m, 2H), 5.82 (m, 1H), 3.82-4.06 (m, 3H), 3.49-3.61 (m, 1H), 3.18 (s, 3H), 2.43-2.62 (m, 2H), 2.24-2.42 (m, 2H). MS (ESI) m/z 493 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834012B2
Source datasetuspto-grants-2010_11
ORD IDord-6ac43cbadbb745ed930ec587cfec67ed
Source noteuspto-grants-2010_11