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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377953Generated: November 1, 2026

Methanol → methyl (Z)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-pentenoate

https://huagongshe.com/reaction/1377953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
Reactant(Z)-2-(2-Aminothiazol-4-YL)-2-pentenoic acidHCID 11344627—
ReactantDimethylaminochloromethyleneammonium chlorideHCID 86750850—
Productmethyl (Z)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-pentenoateHCID 8675085467%

Reaction Steps

Dimethylaminochloromethyleneammonium chloride (830 mg, 6.5 mmol) was added to 12 ml of tetrahydrofuran, and the resulting mixture was ice-cooled. Added to the mixture were 196 mg (0.99 mmol) of (Z)-2-(2-aminothiazol-4-yl)-2-pentenoic acid, followed by stirring for 1 hour. Methanol (10 ml) was added thereto. The mixture so obtained was stirred for 30 minutes. The mixture was then poured into 60 ml of a saturated aqueous solution of sodium hydrogencarbonate. The mixture so obtained was extracted three times with 40 ml portions of ethyl acetate. The extract was dried over anhydrous magnesium sulfate and was then filtered. The filtrate was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column, whereby 177 mg of the title compound were obtained (yield: 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665888
Source datasetuspto-grants-1997_09
ORD IDord-a28970cc80a349caab356b8bddd6d3a7
Source noteuspto-grants-1997_09