Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86652264 | HCID 86652264 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86652263 | HCID 86652263 | — |
Reaction Steps
4-(1-(tert-Butyldimethylsilyloxy)-2-methylpropan-2-yl)-N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)benzamide (4F, 3.9 g, 1.0 equivalent) was dissolved in THF (0.13 M) and treated with TBAF (1.0 M in THF, 4.0 equivalents). After 60 hours, pH 7 phosphate buffer was added and the mixture was extracted with EtOAc. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by chromatography (SiO2, gradient of 25 to 50% EtOAc/hexanes) to give N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(1-hydroxy-2-methylpropan-2-yl)benzamide (4G) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.25 (s, 6 H), 2.44 (s, 3 H), 3.46 (d, J=5.05 Hz, 2 H), 4.76 (t, J=5.31 Hz, 1 H), 6.45 (s, 1 H), 7.52 (d, J=8.59 Hz, 2 H), 7.99 (d, J=8.59 Hz, 2 H), 8.06 (s, 1 H), 11.30 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461163B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-d73906e372e44abeb342a73fa55f4c91 |
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| Source note | uspto-grants-2013_06 |
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