Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 59465201 | HCID 59465201 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25155659 | HCID 25155659 | — |
Reaction Steps
Sodium hydroxide (1 mL, 2M, 2 mmol) was added to a solution of methyl {(7R)-2-amino-8-[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]-6-oxo-5,6,7,8-tetrahydropteridin-7-yl}acetate (272 mg, 0.26 mmol)(Example 7[3]) in methanol (1 mL) and THF (3 mL). The mixture was stirred for 2 hours and then concentrated under reduced pressure. The solution was diluted with water (1 mL) and made acidic by the addition of acetic acid. This solution was loaded onto an SCX column, washed with water and then methanol and the product was eluted with 2M ammonia in methanol. Thus, the title compound was obtained as a cream solid (169 mg, 65%); 1H NMR spectrum (400 MHz, DMSO-d6) δ 2.18 (6H, s), 2.29 (1H, d), 2.38 (1H, d), 3.72 (3H, s), 4.13-4.15 (1H, m), 4.41 (1H, d), 5.49 (1H, d), 5.55 (2H, s), 7.27 (1H, s), 8.13 (1H, s), 9.91 (1H, s); Mass spectrum: (M+H)+ 373.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799781B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-7ca77e954d20445fb7b023a9f010e2e7 |
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| Source note | uspto-grants-2010_09 |
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