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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502243Generated: November 4, 2026

Methanesulfonyl chloride → HCID 59425201, compound

https://huagongshe.com/reaction/502243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 59426180HCID 59426180—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 59425201HCID 5942520181%

Reaction Steps

A solution of 1-ethyl-6-methoxy-1H,1′H-[2,5′]biindolyl-3-carbonitrile (70 mg, 0.22 mmol), prepared as described in Example 1Gb, in pyridine (2 mL) is treated with methanesulfonyl chloride (0.034 mL, 0.44 mmol) and stirred overnight. The reaction mixture is then diluted with H2O and extracted with ethyl acetate (3×). The organic phase is washed with H2O and saturated NaCl, dried and concentrated and purified by flash chromatography using EtOAc/hexanes (30-80%) to afford 70 mg (81%) of 1-ethyl-1′-methanesulfonyl-6-methoxy-1H,1′H-[2,5′]biindolyl-3-carbonitrile as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-473bd4f4c6aa49a2a82b2d8b25818da5
Source noteuspto-grants-2010_08