HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonyl isocyanate → HCID 18973107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | HCID 15228322 | HCID 15228322 | — |
| Reactant | HCID 18973022 | HCID 18973022 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18973107 | HCID 18973107 | — |
Reaction Steps
The title compound was prepared from 5-chloro-3-(2-furoyl)-4-azaoxindole (Example 23) according to the procedure of Example 2C, using 5-chloro-3-(2-furoyl)-4-azaoxindole (200 mg, 0.76 mmol), N-chlorosulfonyl isocyanate (0.10 mL, 1.1 mmol) and acetonitrile (8 mL). Hydrolysis of the N-chlorosulfonyl carboxamide was achieved by quenching the above reaction with water and allowing the mixture to stir at room temperature overnight. The product was collected by filtration and recrystallized from DMSO. Yield: 75 mg (32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811432 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-14c579e251cf452ab252bb9e3b2f2a2f |
| Source note | uspto-grants-1998_09 |