HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(3-amino-1H-indazol-5-yl)-2,6-dichlorobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,6-Dichlorobenzenesulfonylchloride | HCID 522183 | — |
| Reactant | 1H-Indazole-3,5-diamine | HCID 17723727 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-amino-1H-indazol-5-yl)-2,6-dichlorobenzenesulfonamide | HCID 22567053 | 18.6% |
Reaction Steps
N-(3-Amino-1H-indazol-5-yl)-2,6-dichlorobenzenesulfonamide can be obtained as described in Example 39 from 0.8 g of 3,5-diamino-1H-indazole, 8 ml of pyridine, 8 ml of tetrahydrofuran and 1.29 g of 2,6-dichlorobenzenesulfonyl chloride. 350 mg of N-(3-amino-1H-indazol-5-yl)-2,6-dichlorobenzenesulfonamide are thus obtained in the form of a pale yellow solid melting at 250° C. (analysis C13H10Cl2N4O2S % calculated C, 43.71; H, 2.82; Cl, 19.85; N, 15.68; O, 8.96; S, 8.98. % found C, 43.39; H, 2.92; Cl, 19.45; N, 15.31; S, 8.73).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473701B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-5ade5fac7f5b4071b0d66721e2b1aa6b |
| Source note | uspto-grants-2009_01 |