HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2-(5-Nitro-3-sulfamoyl-indol-1-yl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chloride | HCID 22573989 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(5-Nitro-3-sulfamoyl-indol-1-yl)-acetamide | HCID 22574060 | 69% |
Reaction Steps
The 1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chloride (0.37 g, 1.165 mmole) of Step 2 was suspended in methylene chloride (2 ml) and added to ammonium hydroxide (4 ml) at room temperature. After stirring for 2 h at room temperature, the reaction flask was heated on a steam bath for 35 min and then allowed to cool to room temperature. The yellow solid which precipitated was filtered off and dried to afford 0.24 g (0.81 mmole, 69% yield) of 2-(5-nitro-3-sulfamoyl-indol-1-yl)-acetamide. Step 4
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852726B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-cc37e04e2103426789e12188b678ff98 |
| Source note | uspto-grants-2005_02 |