Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18947572 | HCID 18947572 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18947540 | HCID 18947540 | — |
Reaction Steps
The compound from Step E was hydrolysed using THF (2.5 mL), MeOH (0.6 mL) and NaOH (1N, 1.5 mL). The solution was heated at 70° C. for 2 weeks. The reaction was neutralized by addition of Na4OAc buffer (20 mL of 25% w/v) and extracted with EtOAc (3×30 mL). The organic layers were combined, dried over MgSO4, filtered and concentrated. The resulting residue was purified by flash chromatography (eluant:EtOAc-hexane-HOAc (250:750:1)) to give the title compound. Anal. C, H, N for sodium salt·11/2 H2O; Calc. C, 67.70; H, 6.43; N, 4.15 Found C, 67.67; H, 6.31; N, 4.06.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380850 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-22ad331e84f94d7dabb484ecd6d631cf |
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| Source note | uspto-grants-1995_01 |
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