関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | HCID 178448467 | HCID 178448467 | — |
| 反応物 | HCID 178448469 | HCID 178448469 | — |
| 生成物 | HCID 178448470 | HCID 178448470 | 83.9% |
反応手順
The title compound (300 mg, 83%) was prepared from (2R)-2-methyl-2-(methylsulfonyl)-4-[2-oxo-4-(4-{[trans-4-(tetrahydro-2H-pyran-2-yloxy)cyclohexyl]methoxy}phenyl)pyridin-1(2H)-yl]-N-(tetrahydro-2H-pyran-2-yloxy)butanamide (480 mg, 0.726 mmol) by a procedure analogous to that described for (2R)-N-hydroxy-4-[4-{4-[(cis-4-hydroxycyclohexyl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide Example 8, Step F. LCMS m/z 493.7 (M+1)H NMR (400 MHz, DMSO-d6) δ ppm 0.92-1.23 (m, 4 H) 1.54 (s, 3 H) 1.58-1.72 (m, 1 H) 1.81 (br. s., 4 H) 2.06-2.21 (m, 1 H) 2.41 (s, 1 H) 3.08 (s, 3 H) 3.25-3.41 (m, 1 H) 3.74 (br. s., 1 H) 3.80 (d, J=6.44 Hz, 2 H) 3.98-4.17 (m, 1 H) 6.48-6.71 (m, 2 H) 6.85-7.06 (m, 2 H) 7.52-7.78 (m, 3 H) 11.15 (s, 1 H)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846933B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-7c995525808b4dcdb644ac96896f70d0 |
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| 出典メモ | uspto-grants-2014_09 |
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