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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394366Generated: October 29, 2026

Acetonitrile → HCID 18973071, compound

https://huagongshe.com/reaction/2394366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 15228322HCID 15228322—
ReactantHCID 18973048HCID 18973048—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 18973071HCID 18973071—

Reaction Steps

The title compound was prepared from 3-phenylacetyl-6-azaoxindole according to the procedure of Example 2C, using 3-phenylacetyl-6-azaoxindole (1.0 g, 3.9 mmol), N-chlorosulfonyl isocyanate (0.41 mL, 4.7 mmol) and acetonitrile (40 mL). Reaction time: 4 hours. The crude N-chlorosulfonyl carboxamide was hydrolysed by stirring in DMSO (6 mL) for 1 hour in a flask open to the air. After dilution with water, the product was collected by filtration, dried, and recrystallized from acetic acid. Yield: 172 mg (15%). M.p. 131°-133° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811432
Source datasetuspto-grants-1998_09
ORD IDord-d1323a4048644d74a06192be1371b901
Source noteuspto-grants-1998_09