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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394364Generated: October 30, 2026

Chlorosulfonyl isocyanate → HCID 18973116, compound

https://huagongshe.com/reaction/2394364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 15228322HCID 15228322—
ReactantHCID 18973115HCID 18973115—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 18973116HCID 18973116—

Reaction Steps

The title compound was prepared from 5,6-dichloro-3-(2-thenoyl)-4-azaoxindole (Example 6B) according to the procedure of Example 2C, using 5,6-dichloro-3-(2-thenoyl)-4-azaoxindole (194 mg, 0.62 mmol), N-chlorosulfonyl isocyanate (81 L, 0.93 mmol) acetonitrile (10 mL), and a temperature of 50° C. The crude N-chlorosulfonyl carboxamide was hydrolysed by stirring in DMSO in a flask open to the air. After dilution with water, the solid was collected by filtration and recrystallized from acetic acid. Yield: 129 mg (58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811432
Source datasetuspto-grants-1998_09
ORD IDord-3f66f73ef73e4cddb07a73d1cbed2168
Source noteuspto-grants-1998_09