Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 11786402 | HCID 11786402 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 11330169 | HCID 11330169 | — |
Reaction Steps
Ester 7.6 (55 mg, 0.097 mmol) was stirred with 1N LiOH (1 ml) in 4 ml of MeOH/THF (1:3) at rt for 24 h, concentrated, and partitioned between Et2O and H2O. The organic phase was extracted with 0.1 N NaOH (2×), and the combined aqueous extracts were acidified with conc. HCl, and extracted with EtOAc (3×). The combined organic extracts were washed with H2O, brine, and dried (Na2SO4). The crude mixture was purified by semi-preparative HPLC (gradient elution: 70 to 100% CH3CN/H2O+0.1% TFA) to give 7.7, 52 mg (100%). HRMS (ESI) calc'd for C32H30ClN2O4 514.1894, found 541.1913 (MH+); 1H NMR (300 MHz, CDCl3) δ 7.39–7.17 (m, 8H), 7.00–6.94 (m, 3H), 6.51 (s, 1H), 4.95 (s, 2H), 4.14–4.05 (m, 1H), 3.88 (s, 3H), 2.08–1.96 (m, 2H), 1.90–1.86 (m, 4H), 1.26 (br s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112601B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-569d734adfd54ddf9700d1319c80f269 |
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| Source note | uspto-grants-2006_09 |
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