Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 57504523 | HCID 57504523 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57504400 | HCID 57504400 | 56.2% |
Reaction Steps
A solution of tetrabutylammonium fluoride (1M in THF) (1.504 mL, 1.50 mmol) was added dropwise to a stirred solution of (2S)-3-(2-(tert-butyldiphenylsilyloxy)ethoxy)-2-(1-(3-fluoro-2-methylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy)-N-(5-methylpyridin-2-yl)propanamide (Intermediate AF2) (430 mg, 0.61 mmol) in THF (15 mL) over a period of 1 minute and the resulting solution stirred at ambient temperature for 3 hours. Saturated ammonium chloride (20 mL) was added to the reaction mixture which was then diluted with EtOAc (25 mL), and washed sequentially with water (25 mL) and saturated brine (25 mL). The organic layer was dried (MgSO4), filtered and evaporated to afford crude product which was purified by flash silica chromatography, elution gradient 60 to 100% EtOAc in isohexane then by chiral HPLC to afford the product (160 mg, 56%). 1H NMR (400 MHz, DMSO) δ 1.99 (3H, d), 2.24 (3H, s), 3.50-3.56 (2H, m), 3.58-3.68 (2H, m), 4.00-4.05 (1H, m), 4.08-4.13 (1H, m), 4.61 (1H, t), 5.91-5.96 (1H, m), 7.30-7.33 (1H, m), 7.40-7.51 (2H, m), 7.57-7.60 (1H, m), 7.85-7.88 (1H, m), 8.17-8.18 (1H, m), 8.54 (1H, s), 8.61 (1H, s), 10.85 (1H, s); m/z (ESI+) (M+H)+=467; HPLC tR=1.98 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143263B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-dfa3f80f0e5446ccacf14422c1c0d08a |
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| Source note | uspto-grants-2012_03 |
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