HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfate → 1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | (5-Nitro-indol-1-yl)-acetonitrile | HCID 22574036 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chloride | HCID 22573989 | 51% |
Reaction Steps
Chlorosulfonic acid (3.05 ml, 45.9 mmole) from the above Step was added to a suspension of anhydrous sodium sulfate (0.71 g) in methylene chloride (30 ml). After stirring for 25 minutes at room temperature, (5-nitro-indol-1-yl)-acetonitrile (1.00 g) dissolved in methylene chloride was added via syringe. After stirring for 2 h, the reaction mixture was worked up by the cautious addition of ice. When the ice had melted, the mixture was filtered to afford an off-white powder which was washed well with water to afford 0.806 g of 1-carbamoylmethyl-5-nitro-1H-indole-3-sulfonyl chloride (51% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852726B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-1c98694ec1084081892f94b60d78dd43 |
| Source note | uspto-grants-2005_02 |