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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394369Generated: November 2, 2026

Acetonitrile → HCID 18973079, compound

https://huagongshe.com/reaction/2394369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 15228322HCID 15228322—
ReactantHCID 18973030HCID 18973030—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 18973079HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811432
Source datasetuspto-grants-1998_09
ORD IDord-346b5894a84249f29e7858d02daf1ef1
Source noteuspto-grants-1998_09