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Sodium Hydroxide → N-{[(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentyl]carbonyl}-L-valine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | methyl N-{[(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentyl]carbonyl}-L-valinate | HCID 86657845 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-{[(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentyl]carbonyl}-L-valine | HCID 46220211 | 81.4% |
反応手順
To a solution of methyl N-{[(1R,3S,4S)-3-methoxy-4-(nitrooxy)cyclopentyl]carbonyl}-L-valinate (1.04 g, 3.27 mmol) in EtOH (10 mL) was added NaOH (5.0 N, 1.0 mL). After stirring at rt overnight, the mixture was partitioned between Et2O/H2O. The aq layer was extracted and acidified using 5.0 N HCl until pH-3 and then extracted with Et2O (50 mL). The organic layer was washed with brine (2×50 mL), dried over Na2SO4, and concentrated to give the title compound as a white solid (810 mg, yield 81%): 1H NMR (500 MHz, CDCl3) δ 6.70 (d, J=8.4, 1H), 5.40 (d, J=6.0, 1H), 4.53 (dd, J=4.6, 8.5, 1H), 3.93 (m, 1H), 3.48 (s, 3H), 3.03-2.96 (m, 1H), 2.53-2.46 (m, 1H), 2.38-2.20 (m, 3H), 2.08-2.02 (m, 1H), 1.01 (d, J=6.9, 3H), 0.97 (d, J=6.9, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08530521B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-05f34cbbad724863bc6281104eaf4030 |
| 出典メモ | uspto-grants-2013_09 |