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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165270Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 76501932, compound

https://huagongshe.com/reaction/2165270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(alphaZ)-2-Amino-alpha-(methoxyimino)-4-thiazoleacetic acidHCID 5486924—
ReactantHCID 86744079HCID 86744079—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
ProductHCID 76501932HCID 76501932—

Reaction Steps

(S)-[[3-[(Benzyloxycarbonyl)amino]-2-oxo1-azetidinyl]oxy]acetic acid. 1,1-dimethylethyl ester (1.4 g, 4.0 mmol) was dissolved in 25 ml of dry dimethylformamide and hydrogenated with 1 g of 10% palladium on charcoal as catalyst. After 20 minutes the catalyst was filtered and a mixture of (Z)-2-amino-α-(methoxyimino)-4-thiazoleacetic acid (4.4 mmol). 1-hydroxybenzotriazole hydrate (0.15 g, 1.0 mmol). dicyclohexylcarbodiimide (0.81g. 4.4 mmol) and 30 ml of dry dimethylformamide was added. The mixture was stirred overnight at room temperature. The precipitated dicyclohexyl urea was filtered off and the solvent removed in vacuo. The residue was dissolved in ethyl acetate, washed with 5% NaHCO3 and dried over MgSO4. Filtration and evaporation in vacuo gave the title compound which solidified by stirring with ether/petroleum ether; melting point 120° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939253
Source datasetuspto-grants-1990_07
ORD IDord-28a1ba906fad479a99bd6dd50721c93a
Source noteuspto-grants-1990_07