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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569080Generated: October 28, 2026

Methanol → 5-Acetoxymethyl-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/569080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant5-Acetoxymethyl-4-methoxymethyl-1,2,3,4-tetrahydro-beta-carboline-1,3-dicarboxylic acid-3 ethyl esterHCID 20132390—
SolventOxygenHCID 977—
Product5-Acetoxymethyl-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl esterHCID 1385036298.3%

Reaction Steps

90% Azodicarboxylic acid diethyl ester (76 ml) without addition of heat with stirring is added drop by drop to a solution of 5-acetoxymethyl-4-methoxymethyl-1,2,3,4-tetrahydro-beta-carboline-1,3-dicarboxylic acid-3-ethyl ester (75 g) in oxygen-free dichloromethane (0.6 l) under argon protection. The temperature rises about 10° C. Reflux is performed for about 9 hours, then the mixture is left at room temperature for 60 hours. The precipitate is suctioned off, further end product can be obtained from the evaporated mother liquor after chromatography on silica gel with a mixture of dichloromethane (95%) with methanol (5%). Altogether 65 g of the title compound in the form of colorless crystals with a melting point of 129°-133° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731365
Source datasetuspto-grants-1988_03
ORD IDord-c9c8f4abbac041a0bf1cdb8b0633c1d3
Source noteuspto-grants-1988_03