Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178476755 | HCID 178476755 | — |
| Reactant | HCID 178476757 | HCID 178476757 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178503028 | HCID 178503028 | — |
Reaction Steps
Ethyl ((R)-(4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxamido)(phenyl)methyl)phenyl(methyl)phosphinate, 24-f, (18.8 g, 390 mmol) was dissolved in 200 ml of dioxane and treated with 50 ml of 3N NaOH. The mixture was heated at 80° C. for one hour. The mixture was then concentrated under vacuum and the residue was diluted with water and washed with ethyl acetate. The aqueous layer was acidified with conc. HCl to pH=1 and the expected product crashed out, 24-1, (11 g of crude). The product can be further purified via prep-HPLC. 1H NMR (300 MHz, DMSO-d6): δ 8.63 (s, 1H), 8.44 (s, 1H), 8.07 (s, 1H), 7.50 (m, 2H), 7.38 (m, 7H), 6.73 (s, 1H), 6.35 (d, 1H), 1.53 (d, 3H). (M+H)+=450.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079930B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-c43e3228c08444f4b7b0bf0bb63983fd |
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| Source note | uspto-grants-2015_07 |
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