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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757974Generated: November 1, 2026

Methanethiol → 4-Methyl-6-methylthio-beta-carbolin-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/1757974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantSodium MethoxideHCID 10942334—
Reactant6-Bromo-4-methyl-beta-carbolin-3-carboxylic acid ethyl esterHCID 13037328—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-Methyl-6-methylthio-beta-carbolin-3-carboxylic acid methyl esterHCID 86738779—

Reaction Conditions

Temperature100 °C

Reaction Steps

At -10° C. methylmercaptan is introduced into 150 ml of tetrahydrofuran. Within 2 hours, at -10° C., 100 ml of 1.6 molar butyl lithium solution (hexane) is added dropwise thereto. The whole is then stirred for 30 minutes and the solvent is then distilled off in vacuo at a bath temperature of 20° C. The lithium methylmercaptide thus prepared is dissolved in 100 ml of N-methylpyrrolidone. 10.2 g of 6-bromo-4-methyl-β-carbolin-3-carboxylic acid ethyl ester is added thereto, and the whole is heated for 24 hours under argon protecting gas for 24 hours at 100° C. For work-up, the mixture is stirred into 400 ml of ice water, extracted with ethyl acetate, and the extracts are washed with water until neutral. The crude product obtained in this manner is dissolved in 250 ml of methanol and after the addition of 1 g of sodium methylate, is boiled for 6 hours. The solvent is then distilled off in vacuo, 150 ml of saturated sodium hydrogen phosphate solution is added to the residue and extraction with ethyl acetate is carried out. After washing with water until neutral, drying with sodium sulphate, filtering and distilling off the solvent, 8.85 g of 4-methyl-6-methylthio-β-carbolin-3-carboxylic acid methyl ester is obtained, which is crystallized from diisopropyl ether. Melting point 186°-193° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371536
Source datasetuspto-grants-1983_02
ORD IDord-caa14f1de5e94c6d87c0e7cc43421d0d
Source noteuspto-grants-1983_02