HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → N-(2-Benzoyl-6-Chloro-1H-Indol-3-Yl)4-Methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 3-Amino-2-benzoyl-6-chloro-1-(ethoxycarbonyl)indole | HCID 18367833 | — |
| Product | N-(2-Benzoyl-6-Chloro-1H-Indol-3-Yl)4-Methylbenzenesulfonamide | HCID 9932168 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 33 from ethyl 3-amino-2-benzoyl-6-chloro-1H-indole-1-carboxylate (Example 1, step 2) and p-toluenesulfonyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277878B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-42af586597c74fc3b8878bc11e69d17c |
| Source note | uspto-grants-2001_08 |