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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877636Generated: October 30, 2026

Hydrazine → 3-(hydrazinecarbonyl)-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/877636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantMethyl 3-(methylsulfamoyl)benzoateHCID 9320906—
SolventMethanolHCID 887—
Product3-(hydrazinecarbonyl)-N-methylbenzenesulfonamideHCID 6775135074.3%

Reaction Conditions

Temperature65 °C

Reaction Steps

Hydrazine (43.3 mg, 1.352 mmol) was added to the methyl 3-(N-methylsulfamoyl)benzoate (155 mg, 0.676 mmol) in methanol and refluxed for 12 h at 65° C. Following cooling, reaction was monitored by TLC. After completion of the reaction, the solvent was removed by vacuum and then compound was purified by column chromatography to yield 3-(hydrazinecarbonyl)-N-methylbenzenesulfonamide (120 mg, 0.502 mmol, 74.3% yield). 1H NMR (CDCl3, 400 MHz): δ 8.25 (m, 1H), 8.01 (m, 2H), 7.64 (m, 2H), 4.63 (m, 1H), 4.17 (m, 2H), 2.69 (d, 3H, J=5.2 Hz). ESI-MS: 230.0 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987335B2
Source datasetuspto-grants-2015_03
ORD IDord-7289578c2e3848d48293581869ea2cb4
Source noteuspto-grants-2015_03