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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502139Generated: October 25, 2026

Chlorosulfonyl isocyanate → 6-methoxy-2-methyl-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/502139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantSodium BicarbonateHCID 516892—
Reactant6-methoxy-2-methyl-1H-indoleHCID 10844709—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product6-methoxy-2-methyl-1H-indole-3-carbonitrileHCID 1390464081%

Reaction Steps

To a solution of 6-methoxy-2-methyl-1H-indole (3.9 g, 24 mmol) in acetonitrile (200 mL) and DMF (20 mL) is added dropwise a solution of ClSO2NCO (4 mL, 1.3 eq.) in acetonitrile (31 mL) at 0° C. After the addition, the mixture is stirred at room temperature for 3 h. Then it is poured into ice water and saturated NaHCO3 is added to it until it becomes basic. The aqueous phase is extracted with CH2Cl2 and then evaporated. The residue is purified with flash column chromatography on silica gel using EtOAc/petroleum ether (1/5) as eluent to yield 81% of 6-methoxy-2-methyl-1H-indole-3-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-0aec329a041b43c0bd4bedc4b9fe0881
Source noteuspto-grants-2010_08