HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165270Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 76501932, compound
https://huagongshe.com/reaction/2165270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | (alphaZ)-2-Amino-alpha-(methoxyimino)-4-thiazoleacetic acid | HCID 5486924 | — |
| Reactant | HCID 86744079 | HCID 86744079 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 76501932 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939253 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-28a1ba906fad479a99bd6dd50721c93a |
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| Source note | uspto-grants-1990_07 |
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