Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-[3-(6-Amino-pyridin-3-ylethynyl)-2-ethyl-pyridin-4-yl]-2-fluoro-benzoic acid methyl ester | HCID 58235283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58235232 | HCID 58235232 | — |
Reaction Steps
The title compound is synthesized according to general procedure GP4 starting from 2.36 g (6.3 mmol) 4-[3-(6-Amino-pyridin-3-ylethynyl)-2-ethyl-pyridin-4-yl]-2-fluoro-benzoic acid methyl ester (A-37) using 9.4 mL (9.4 mmoL) 1N NaOH in 40 mL THF. The reaction mixture is stirred for 2 h at 95° C. The solvent is removed under reduced pressure, the crude product is taken up with water and the pH is adjusted to 5 (with 1N HCl). The precipitate is collected by filtration. Yield after drying: 2.2 g (97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090564B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-77b16910e93e43ab941c0c146ecf36b6 |
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| Source note | uspto-grants-2015_07 |
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