Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10769651 | HCID 10769651 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10529227 | HCID 10529227 | 71.2% |
Reaction Steps
To a mixture of p-methoxybenzyl (6R,7R)-7-phenylacetamido-3-(trifluoromethylsulphonyloxy)ceph-3-em-4-carboxylate (20 mg, 0.0341 mmol), allyl alcohol (11.6 μl, 0.171 mmol) and dichloromethane (0.5 ml) was added diisopropylethyl-amine (6 μl, 0.034 mmol). After stirring at room temperature for 30 min the mixture was chromatographed to give the title compound (12 mg, 71%), (Found: M+, 4.94.1528. C26H26N2O6S requires M, 494.1512); νmax (CH2Cl2) 1787, 1722, 1687 cm-1 ; δH (CDCl3) 2.89 (1H, m), 2.96 (1H, dt, J 16.8 , 3.0), 3.22 (1H, ddd, J 16.2, 8.9, 1.2), 3.62 (2H, ABq, J 15.7), 3.65 (2H, d, J 7.2), 3.79 (3H, s), 4.44 (1H, m), 4.92 (1H, d, J 5.0), 5.17 (2H, ABq, J 12.0), 5.76 (1H, dd, J 8.9, 5.0), 6.32 (1H, d, J 8.9), 6.86 (2H, d, J 8.6), 7.28 (7H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05578592 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-abf8c259008d47cbb321c1a3a8ec5fb8 |
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| Source note | uspto-grants-1996_11 |
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