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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720326Generated: November 2, 2026

Dichloromethane → 5-(2-Chlorobenzyl)-4-methoxymethyl-9-tosyl-beta-carboline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1720326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant5-(4-Chlorobenzyl)-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl esterHCID 54002862—
Product5-(2-Chlorobenzyl)-4-methoxymethyl-9-tosyl-beta-carboline-3-carboxylic acid ethyl esterHCID 53990242—

Reaction Steps

0.744 g (0.0039 mol) of p-toluenesulfochloride is added under ice cooling to a solution of 1.2 g (0.0029 mol) of 5-(4-chlorobenzyl)-4-methoxymethyl-β-carboline-3-carboxylic acid ethyl ester, 0.16 g (0.0013 mol) of dimethylaminopyridine and 0.54 ml (0.0039 mol) of triethylamine in 120 ml of dichloromethane. The reaction mixture is stirred for another 15 minutes under ice cooling and then for 2 hours at room temperature. Then it is diluted with dichloromethane, washed with water, dried and concentrated by evaporation. The evaporation residue is crystallized under trituration with ether. The yield is 1.36 g (82% of theory) of 5-(2-chlorobenzyl)-4-methoxymethyl-9-tosyl-β-carboline-3-carboxylic acid ethyl ester, melting point 140°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506234
Source datasetuspto-grants-1996_04
ORD IDord-abc7e3116cf34163aa8095bd0ae078c7
Source noteuspto-grants-1996_04