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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906717Generated: November 2, 2026

2-Aminothiophenol → HCID 13763167, compound

https://huagongshe.com/reaction/1906717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantMethyl 2-benzylideneacetoacetateHCID 2884254—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 13763167HCID 13763167—

Reaction Steps

A solution of 2-[(phenyl)methylene]-3-oxobutanoic acid, methyl ester (13.0 g., 63.7 mmole) in dry dimethylformamide (20 ml.) is treated dropwise with 2-aminothiophenol (8.85 g. of 90%, 63.7 mmole). A slight release of heat is noted. The reaction is stirred at room temperature for 6 hours and then heated at 65° for 72 hours. It is cooled to room temperature and diluted with ether. The resulting solution is thoroughly washed with water, sodium bicarbonate and brine. After drying over anydrous magnesium sulfate, the solvent is stripped off to give a yellow solid. It is triturated with isopropyl ether and filtered off to provide 6.93 g. of light yellow crystals. Recrystallization from isopropyl ether-dichloromethane gives an analytically pure sample of 2,5-dihydro-4-methyl-2-phenyl-1,5-benzothiazepine-3-carboxylic acid, methyl ester; m.p. 154°-156°. TLC(silica gel, hexane:acetone, 70:30) Rf =0.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654335
Source datasetuspto-grants-1987_03
ORD IDord-e5cd192ec9e54dd0baa06693071d8405
Source noteuspto-grants-1987_03