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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192123Generated: October 31, 2026

5-((3,5-Dichloropyridin-4-yl)thio)-4-nitrothiophene-2-carbonyl chloride → 5-((3,5-dichloropyridin-4-yl)thio)-N-(4-(methylsulfonyl)benzyl)-4-nitrothiophene-2-carboxamide

https://huagongshe.com/reaction/1192123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-((3,5-Dichloropyridin-4-yl)thio)-4-nitrothiophene-2-carbonyl chlorideHCID 60207337—
Reactant4-Methylsulfonyl-benzylamine hydrogen chloric acid saltHCID 86664724—
Product5-((3,5-dichloropyridin-4-yl)thio)-N-(4-(methylsulfonyl)benzyl)-4-nitrothiophene-2-carboxamideHCID 60207339—

Reaction Steps

Prepared according to the procedure described for example 50 from 5-[(3,5-dichloro-4-pyridyl)sulfanyl]-4-nitro-thiophene-2-carbonyl chloride (100 mg, 0.27 mmol) and 4-methylsulfonyl-benzylamine hydrogen chloric acid salt (59 mg, 0.32 mmol). The title compound was obtained as a yellow solid (54 mg, 39% yield). 1H NMR (400 MHz, d6-DMSO) δ: 9.51 (1H, m), 8.99 (2H, s), 8.48 (1H, s), 7.89 (2H, dd), 7.55 (2H, dd), 4.51 (2H, m), 3.18 (3H, s). MS m/z: 515.97, 517.99 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680139B2
Source datasetuspto-grants-2014_03
ORD IDord-ee1950fcb89441e79276fcc814bae183
Source noteuspto-grants-2014_03