HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 178491510, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 14071104 | HCID 14071104 | — |
| Reactant | HCID 14621694 | HCID 14621694 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178491510 | HCID 178491510 | 35.5% |
Reaction Steps
(Z)-2-(2-tritylaminothiazol-4-yl)-2-tetrahydropyranyloxyiminoacetic acid (0.39 g, 0.76 mmol) and p-methoxybenzyl 7-amino-3-[(Z)-2-(1,2,3-thiadiazol-4-yl)vinyl]-3-cephem-4-carboxylate (1.33 g, 0.76 mmol) were dissolved in methylene chloride (10 ml) and stirred at room temperature for 12 hours by addition of DCC (0.18 g, 0.87 mmol). Insolubles were filtered and then the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography thereby p-methoxybenzyl 7-[(Z)-2-(2-tritylaminothiazol-4-yl)-2-tetrahydropyranyloxyiminoacetamido]-3-[(Z)-2-(1,2,3-thiadiazol-4-yl)vinyl]-3-cephem-4-carboxylate (0.25 g) was obtained as a light yellow powder compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05073551 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-96414e54e4ef4a60a21e7510bdb15525 |
| Source note | uspto-grants-1991_12 |