HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(3-amino-1H-indazol-5-yl)-2,6-difluorobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,6-Difluorobenzenesulfonyl chloride | HCID 2734271 | — |
| Reactant | 1H-Indazole-3,5-diamine | HCID 17723727 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-amino-1H-indazol-5-yl)-2,6-difluorobenzenesulfonamide | HCID 22567087 | 8.4% |
Reaction Steps
N-(3-Amino-1H-indazol-5-yl)-2,6-difluorobenzenesulfonamide can be obtained as described in Example 39 from 1 g of 3,5-diamino-1H-indazole, 10 ml of pyridine, 10 ml of tetrahydrofuran and 1.4 g of 2,6-difluorobenzenesulfonyl chloride. 179 mg of N-(3-amino-1H-indazol-5-yl)-2,6-difluorobenzenesulfonamide are thus obtained in the form of a gray solid melting at 241° C. (analysis C13H10F2N4O2S % calculated C, 48.15; H, 3.11; F, 11.72; N, 17.28; O, 9.87; S, 9.89. % found C, 47.81; H, 3.18; F, 11.64; N, 17.00; S, 9.67).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473701B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-5b960d4392684a8d93b7cddafda633c5 |
| Source note | uspto-grants-2009_01 |