HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032192Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 16166018, compound
https://huagongshe.com/reaction/1032192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 13821813 | HCID 13821813 | — |
| Reactant | HCID 14050777 | HCID 14050777 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16166018 | HCID 16166018 | — |
Reaction Steps
To an ice-cooled solution of the crude product obtained in Step 5 (5.6 g) and (6R,7R)-7-amino-3-[(2-diphenylmethyloxycarbonyl-5-methyl-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester (5.0 g) in dichloromethane (170 ml) was added dicyclohexylcarbodiimide (1.4 g), and the mixture was stirred at room temperature for five hours. After filtering off the insoluble matters, the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and the insoluble matters were filtered off. The filtrate was washed with brine and dried over anhydrous sodium sulfate. The dried solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography, giving 0.73 g (less polar form) and 1.39 g (more polar form) of the objective compounds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04956474 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-3ef44d455375476c99232ea67437d929 |
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| Source note | uspto-grants-1990_09 |
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