benzyl 4-((1R,2S)-2-(2-(5-(methylsulfonyl)pyridin-2-yloxy)ethyl)cyclopropyl)piperidine-1-carboxylate → 5-(methylsulfonyl)-2-{2-[(1S,2R)-2-piperidin-4-ylcyclopropyl]ethoxy}pyridine
反応式
[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:11][CH2:12][CH2:13][C@@H:14]2[CH2:16][C@@H:15]2[CH:17]2[CH2:22][CH2:21][N:20](C(OCC3C=CC=CC=3)=O)[CH2:19][CH2:18]2)=[N:9][CH:10]=1)(=[O:4])=[O:3]>[Pd].C(O)C>[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:11][CH2:12][CH2:13][C@@H:14]2[CH2:16][C@@H:15]2[CH:17]2[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]2)=[N:9][CH:10]=1)(=[O:3])=[O:4]参加物
実験手順
Benzyl 4-((1R,2S)-2-(2-(5-(methylsulfonyl)pyridin-2-yloxy)ethyl)cyclopropyl)piperidine-1-carboxylate (Intermediate 12; 1.20 g, 2.62 mmol) and palladium on activated carbon (10%, wet, 240 mg) in ethanol (50 mL) were stirred under an atmosphere of hydrogen (1 atm) at RT for 3 h. The mixture was filtered (glass wool filter paper, Whatman 1821 110), and washed with ethanol. The filtrate was concentrated to dryness under reduced pressure to provide the title compound as an off-white solid. 1H NMR (300 MHz, CDCl3) δ 8.72 (dd, J=0.5, 2.5 Hz, 1H), 8.03 (dd, J=2.5, 8.7 Hz, 1H), 6.84 (dd, J=0.6, 8.7 Hz, 1H), 4.48 (t, J=7.2 Hz, 2H), 3.20-3.05 (m, 2H), 3.07 (s, 3H), 2.65-2.50 (m, 2H), 2.20-1.90 (m, 2H), 1.85-1.65 (m, 2H), 1.60-1.45 (m, 1H), 1.45-1.20 (m, 2H), 1.00-0.80 (m, 2H), 0.70-0.60 (m, 2H), −0.13 (q, J=4.2 Hz, 1H). MS (Multimode) m/z 325 [M+H]+.
後処理
- filtrationThe mixture was filtered
- filtration(glass wool filter paper, Whatman 1821 110)
- washwashed with ethanol
- concentrationThe filtrate was concentrated to dryness under reduced pressure
出典と根拠
- ORDレコード
- ord-94170d942a3643819e1314057a0345a9
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08957062B2
反応ノート
読み込み中…