HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249605Generated: October 27, 2026
Dicyclohexylcarbodiimide → HCID 178525025, compound
https://huagongshe.com/reaction/249605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (-)-Mandelic acid | HCID 11914 | — |
| Reactant | HCID 178511753 | HCID 178511753 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178525025 | HCID 178525025 | 49.5% |
Reaction Steps
To a solution of 7β-amino-3-(trityl-1,2,3-triazol-4-ylthiomethylthio) -3-cephem-4-carboxylic acid diphenylmethyl ester (800 mg : 1.06 mMol.) and D-(-)-mandelic acid (242 mg 1.59 mMol.) in dichloromethane (4 ml) is added dicyclohexylcarbodiimide (328 mg : 1.59 mMol.}, and the mixture is stirred under ice cooling for 1 hour. The reaction mixture is concentrated, diluted with ethyl acetate, and filtered to remove solid. The filtrate is washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue is purified by Lobar column chromatography (toluene : ethyl acetate=2:1) to give 7β-D-mandelamido-3-(trityl-1,2,3-triazol-4-ylthiomethylthio) -3-cephem- 4-carboxylic acid diphenylmethyl ester (466 mg) as yellow foam. Yield : 50%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05214037 |
|---|
| Source dataset | uspto-grants-1993_05 |
|---|
| ORD ID | ord-6a1e5c545b44408db188588735deab15 |
|---|
| Source note | uspto-grants-1993_05 |
|---|