HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydrazinylbenzenesulfonamide hydrochloride → HCID 178514744, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydrazinylbenzenesulfonamide hydrochloride | HCID 2794567 | — |
| Reactant | 4-nitro-1H-indole-2,3-dione | HCID 11745463 | — |
| Product | HCID 178514744 | HCID 178514744 | 33% |
Reaction Steps
The title compound was prepared from 4-nitro-1H-indole-2,3-dione (Gassman, et al., Journal of Organic Chemistry 1977, 42, 1344-8) and 4-sulfonamidophenylhydrazine hydrochloride according to Procedure G in 33% yield: 1H NMR (DMSO-d6): δ7.23 (d, J=7.7 Hz, 1H), 7.31 (s, 2H), 7.47 (t, J=7.9 Hz, 1H), 7.56 (d, J=7.9 Hz, 2H), 7.59 (d, J=7.2 Hz,1H), 7.83 (d, J=7.7 Hz, 2H), 11.59 (s, 1H), 13.20 (s, 1H); APCI−MS m/z 361 (M)−. Anal. Calcd for C14H11N5O5S: C, 46.54, H, 3.07; N, 19.38; S, 8.87. Found C, 46.62, H, 3.09; N, 19.46; S. 8.81.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06369086B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-8a2c60bb591c4caa854f2fbbd2c4dc8b |
| Source note | uspto-grants-2002_04 |