Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | (3-Methoxyphenyl)boronic acid | HCID 2734370 | — |
| Reactant | N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide | HCID 86652272 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67064353 | HCID 67064353 | 9% |
Reaction Steps
A suspension of N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2D, 50 mg, 151 mmol), 3-methoxyphenylboronic acid (46 mg, 302 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (9 mg, 12 μmol) in 2:1 1,4-dioxane/saturated aqueous NaHCO3 (670 microliters of 1,4-dioxane and 330 microliters of saturated aqueous NaHCO3) was prepared in a 2 mL microwave reaction vessel and the sealed reaction vessel warmed to 110° C. for 20 minutes. The reaction mixture was cooled to rt, diluted with methanol, filtered, and purified via preparative HPLC, 45-70% (MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a yellow solid (5.2 mg, 9%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.46 (s, 6 H) 3.85 (s, 3 H) 6.59 (d, J=2.27 Hz, 1 H) 7.22 (dd, J=8.08, 1.77 Hz, 1 H) 7.55 (t, J=7.83 Hz, 1 H) 7.59-7.70 (m, 4 H) 7.98-8.09 (m, 3 H) 8.20 (d, J=2.02 Hz, 1 H) 11.27 (s, 1 H). ESI-MS: m/z 403.3 (M+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-8f31775931a54d56bb2e9a34e4c615a7 |
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| Source note | uspto-grants-2013_06 |
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