HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → N-[amino-(4-methylpiperazin-1-yl-amino)-methylene]-4-methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1-Amino-4-methylpiperazine | HCID 81349 | — |
| Reactant | N-[(3,5-dimethylpyrazol-1-yl)-iminomethyl]-4-methylbenzene-sulfonamide | HCID 178427489 | — |
| Product | N-[amino-(4-methylpiperazin-1-yl-amino)-methylene]-4-methylbenzenesulfonamide | HCID 67176487 | — |
Reaction Steps
The compound of Example 8 was prepared according to the accompanying synthesis procedure from 0.5 ml of N-[(3,5-dimethylpyrazol-1-yl)-iminomethyl]-4-methylbenzene-sulfonamide solution (0.2 M, acetonitrile) with 19 mg of methanesulfonic acid and 0.5 ml of N-amino-4-methylpiperazine solution (1.0 M, acetonitrile) and filed in a substance databank. Calculated mol. wt. 311.40; found mol. wt. (M+H) 312.2; 623.0 (Dimer)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07671074B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-b609d3a693cb4dc0841e06621dc67c6a |
| Source note | uspto-grants-2010_03 |