Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873668Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 66850754, compound

https://huagongshe.com/reaction/873668

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 numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-c73201a554b94b49bba0063994078d13
Source noteuspto-grants-2015_03