Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 11146426 | HCID 11146426 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54008737 | HCID 54008737 | — |
Reaction Steps
To a stirred solution of ethyl 2-(2',3',5'-tri-O-benzoyl-β-D-ribofuranosyl)thiazole-4-carboxylate 8 (3.01 g, 5.00 mmol) in dry ethanol (50 ml) under argon atmosphere was added NaOEt (1.02 g, 15 mmol) powder. The reaction mixture was stirred at room temperature overnight, neutralized with Dowex 50W-X8 H+ resin and filtere. The resin was washed with ethanol (20 ml) and the filtrate evaporated to dryness. The residue was dissolved in salt free water (50 ml) and washed with CHCl3 (2×50 ml). The water extract was evaporated to dryness under reduced pressure to an oil. The oil was dissolved in minimum amount of warm ethyl acetate (10 mL). The solution was seeded with authentic 5 and once crystallization had begun the mixture was refrigerated (5° C.) for 16 h. The solid was collected by filtration, washed with cold (5° C.) ethyl acetate (5 mL), and dried (40° C., 1 mm); 1.2 g (83%), mp 74-78° C. 1H NMR (DMSO-d6): d 1.31 (t, 3H), 3.46-3.64 (m, 2H), 3.8-4.12 (m, 3H), 4.30 (q, 2H), 4.84 (t, 1H) 4.94 (d, 1H), 5.04 (d, 1H), 5.4 (d,1H) and 8.49 (s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05907036 |
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| Source dataset | uspto-grants-1999_05 |
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| ORD ID | ord-45eb60ee7f7543328e7c42cd434f3a9f |
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| Source note | uspto-grants-1999_05 |
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