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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515467Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 66850754, compound

https://huagongshe.com/reaction/1515467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylateHCID 1756750—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66850754HCID 66850754—

Reaction Steps

A solution of 3 g of 1,3,4,5-tetrahydro-pyrido[4,3-b]indole-2-carboxylic acid ethyl ester in methylene chloride (50 mL) is treated with 0.982 g of sodium hydroxide and stirred and room temperature overnight. Benzenesulfonylchloride (6.30 mL) is added to the reaction and stirred at room temperature overnight. The reaction mixture is diluted with water (250 mL) and extracted with methylene chloride. The organics are combined, washed with water then a saturated sodium chloride solution, dried over sodium sulfate and concentrated in vacuo. The residue is loaded on Celite and purified by silica gel chromatography (1:1 hexanes/ethyl acetate) to give 5-benzenesulfonyl-1,3,4,5-tetrahydro-pyrido[4,3-b]indole-2-carboxylic acid ethyl ester as a yellow powder. MS (m/z): 385 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222424B2
Source datasetuspto-grants-2012_07
ORD IDord-d23ed09c51864283b6926d07cb550896
Source noteuspto-grants-2012_07