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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296793Generated: October 30, 2026

Diisopropylethylamine → HCID 178516947, compound

https://huagongshe.com/reaction/1296793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantRhodanineHCID 1201546—
ReactantTranylcypromine hydrochlorideHCID 2723716—
SolventAcetonitrileHCID 6342—
ProductHCID 178516947HCID 17851694742%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of (1R,2S)-2-phenyl-cyclopropylamine hydrochloride (0.85 g, 5 mmol) and Rhodanine (0.68 g, 5 mmol) in acetonitrile (20 mL) was added DIPEA (2.61 mL, 15 mmol) at room temperature. Then, this solution was cooled to 0° C. and mercuric chloride (1.35 g, 5 mmol) was added in two portions within a period of 10 min. After addition, the suspension was allowed to warm to room temperature and stirred for 2 days. The resulting black solids were filtered through a plug of celite and washed with ethyl acetate (500 mL). The solvent was removed under the vacuum and the crude residue was diluted with water (100 mL) and ethyl acetate (100 mL). The two layers were separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic extracts were washed with brine solution and dried over anhydrous magnesium sulfate. Filtration of the drying agent and removal of the solvent under the vacuum gave the crude residue which was purified by using a Biotage silica gel column chromatography to obtain 0.474 g (42% yield) of 2-((1R,2S)-2-phenyl-cyclopropylamino)-thiazol-4-one was isolated as a white amorphous solid: EI-HRMS m/e calcd for C12H12N2OS (M+) 232.0670. found 232.0665.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247727B2
Source datasetuspto-grants-2007_07
ORD IDord-0b4acc7f5c3e4e89b4f45a4a98c759e6
Source noteuspto-grants-2007_07