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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483975Generated: October 30, 2026

Water → 2-(1-Amino-1-methylethyl)-4,5-bis(4-methoxyphenyl)thiazole hydrochloride

https://huagongshe.com/reaction/483975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Chloro-1,2-bis(4-methoxyphenyl)ethan-1-oneHCID 3862523—
Reactanttert-butyl N-(1-carbamothioyl-1-methylethyl)carbamateHCID 15186362—
SolventDimethylformamideHCID 6228—
Product2-(1-Amino-1-methylethyl)-4,5-bis(4-methoxyphenyl)thiazole hydrochlorideHCID 1974890281.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1,2-bis(4-methoxyphenyl)-2-chloroethanone (5.00 g) and 2-tert-butyloxycarbonylamino-2-methylpropanethioamide (4.50 g) in dimethylformamide (25 ml) was stirred at 70° C. for 6 hours. After allowing to cool to the ambient temperature, the reaction mixture was dropped into water. The precipitates were collected by filtration. The resulting residue (6.28 g) was dissolved with dichloromethane (120 ml), and stirred at 2° C. To the reaction mixture was added 1,4-dioxan solution of 4N hydrogen chloride (60 ml), and stirred at ambient temperature for 1 hour. The resulting residue was evaporated in vacuo. The residue was added iso-propyl ether (300 ml) and stirred at 2° C. for 3 hours. The resulting precipitate was collected by filtration and washed with iso-propyl ether, to give 2-(1-amino-1-methylethyl)-4,5-bis(4-methoxyphenyl)thiazole hydrochloride (5.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229386
Source datasetuspto-grants-1993_07
ORD IDord-c0b22498621a4c2cbe4b8f6c1dc95c8a
Source noteuspto-grants-1993_07