HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 18973079, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | HCID 15228322 | HCID 15228322 | — |
| Reactant | HCID 18973030 | HCID 18973030 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 18973079 | HCID 18973079 | — |
Reaction Steps
The title compound was prepared from 3-benzoyl-5-chloro-4-azaoxindole (Example 32) according to the procedure of Example 25, using 3-benzoyl-5-chloro-4-azaoxindole (2.73 g, 10.0 mmol), N-chlorosulfonyl isocyanate (1.3 mL, 15 mmol) and acetonitrile (80 mL). The reaction time was 20 hours. The crude N-chlorosulfonyl carboxamide was hydrolyzed by stirring in DMSO (15 mL) for 20 hours. The crude product was recrystallized from acetic acid and washed with methanol. Yield: 0.36 g (11%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811432 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-346b5894a84249f29e7858d02daf1ef1 |
| Source note | uspto-grants-1998_09 |