HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877636Generated: October 30, 2026
Hydrazine → 3-(hydrazinecarbonyl)-N-methylbenzenesulfonamide
https://huagongshe.com/reaction/877636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Methyl 3-(methylsulfamoyl)benzoate | HCID 9320906 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(hydrazinecarbonyl)-N-methylbenzenesulfonamide | HCID 67751350 | 74.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987335B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-7289578c2e3848d48293581869ea2cb4 |
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| Source note | uspto-grants-2015_03 |
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