Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Benzoic acid, 3-(aminosulfonyl)-, methyl ester | HCID 108836 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71258151 | HCID 71258151 | 50.9% |
Reaction Steps
Methyl 3-sulfamoylbenzoate (110 mg, 0.511 mmol) was added to the hydrazine (32.8 mg, 1.022 mmol) in methanol and refluxed for 8 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 flash chromatography (5% methanol/DCM) to yield the 3-(hydrazinecarbonyl)benzenesulfonamide (57 mg, 0.260 mmol, 50.8% yield) as a white solid. 1H NMR (CD3OD, 400 MHz): δ 8.32 (m, 1H), 8.04 (d, 1H, J=7.6 Hz), 7.97 (d, 1H, J=7.6 Hz), 7.63 (t, 1H, J=8.0 Hz). Mass [M+H]+:216.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08987335B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-1284525798bd4ea7aea67168f1706239 |
|---|
| Source note | uspto-grants-2015_03 |
|---|