Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | (E)-2-benzyloxy-3-hydroxy-but-2-enedioic acid 4-tert-butyl ester | HCID 86725882 | — |
| Reactant | Acetic acid;2-(1-pyrrolo[2,3-b]pyridin-1-ylcyclopentyl)ethanimidamide | HCID 86726064 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178450821 | HCID 178450821 | 75.4% |
Reaction Steps
To a stirred solution of 2-(1-pyrrolo[2,3-b]pyridin-1-yl-cyclopentyl)-acetamidine; compound with acetic acid (402) (800 mg, 2.65 mmol) and (E)-3-benzyloxy-2-hydroxy-4-oxo-pent-2-enoic acid tert-butyl ester (4) (978 mg, 3.18 mmol) in methanol (80 mL) was added sodium methoxide solution (25% in methanol) (1.7 mL, 7.94 mmol) at 0° C. The reaction mixture was allowed to warm slowly to room temperature and was stirred for 16 h (TLC, ethyl acetate, Rf=0.3). After completion of the reaction, methanol was evaporated to get a crude product which was purified by Combi-Flash column (eluted at 60-70% ethyl acetate in hexane) to get 5-benzyloxy-6-hydroxy-2-(1-pyrrolo[2,3-b]pyridin-1-yl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid tert-butyl ester (403) (1 g, 75%) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045486B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-be57e476fb8a44d0b36bd91b73511355 |
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| Source note | uspto-grants-2015_06 |
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