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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394358Generated: November 1, 2026

Chlorosulfonyl isocyanate → HCID 18973107, compound

https://huagongshe.com/reaction/2394358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 15228322HCID 15228322—
ReactantHCID 18973022HCID 18973022—
SolventAcetonitrileHCID 6342—
ProductHCID 18973107HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811432
Source datasetuspto-grants-1998_09
ORD IDord-14c579e251cf452ab252bb9e3b2f2a2f
Source noteuspto-grants-1998_09