HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028030Generated: October 30, 2026
Chlorosulfonyl isocyanate → HCID 66730841, compound
https://huagongshe.com/reaction/1028030
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | HCID 66730861 | HCID 66730861 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66730841 | HCID 66730841 | — |
Reaction Steps
To a solution of (S)-6-(6-ethyl-5-fluoro-1H-indol-2-yl)-N-(1,1,1-trifluoropropan-2-yl)pyridine-3-sulfonamide (0.22 g, 0.53 mmol) in a mixture of DMF (0.5 mL) and acetonitrile (0.5 mL) was added chlorosulfonyl isocyanate dropwise at −50° C. The reaction mixture was kept stirring at 0° C. for 0.5 hr and then quenched with ice, following by pouring into water. After 0.5 hr stirring at room temperature, the resulting solid was collected by filtration and washed with water, hexane and CH2Cl2. After air drying, (S)-6-(3-cyano-6-ethyl-5-fluoro-1H-indol-2-yl)-N-(1,1,1-trifluoropropan-2-yl)pyridine-3-sulfonamide was obtained and used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08735414B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-f9946d89fb3c4a28a506004b043a5747 |
|---|
| Source note | uspto-grants-2014_05 |
|---|