反応式
C1C2C(COC([NH:18][C@H:19]([C:46]([OH:48])=[O:47])[CH2:20][CH2:21][CH2:22][CH2:23][NH:24][C:25](=[O:45])[CH2:26][CH2:27][CH:28]([P:37]([CH2:42][CH:43]=[CH2:44])([CH2:39][CH:40]=[CH2:41])=[O:38])[P:29]([CH2:34][CH:35]=[CH2:36])([CH2:31][CH:32]=[CH2:33])=[O:30])=O)C3C(=CC=CC=3)C=2C=CC=1>N1CCCCC1.CN(C=O)C.C(OCC)(=O)C>[CH2:31]([P:29]([CH:28]([P:37]([CH2:39][CH:40]=[CH2:41])([CH2:42][CH:43]=[CH2:44])=[O:38])[CH2:27][CH2:26][C:25]([NH:24][CH2:23][CH2:22][CH2:21][CH2:20][C@@H:19]([C:46]([OH:48])=[O:47])[NH2:18])=[O:45])([CH2:34][CH:35]=[CH2:36])=[O:30])[CH:32]=[CH2:33]参加物
実験手順
A solution of 90 (502 mg, 0.616 mmol) in piperidine/DMF (0.05:1, 5 mL) was stirred at room temperature for 18 hr. After diluting with ethyl acetate (40 mL) the organic layer was washed with water and brine then dried over Na2SO4 and concentrated in vacuo. The crude material was purified by silica gel chromatography (methanol in ethyl acetate, 5% over 5 column volumes then 5 to 30% over 10 column volumes) using a Biotage Horizon™ apparatus resulting in the colourless liquid 91 (249 mg, 68%): 1H NMR (400 MHz, CDCl3) δ 1.39-1.74 (m, 6H), 1.45 (s, 9H), 2.21-2.35 (m, 2H), 2.51 (t, J=7.4, 2H), 2.55 (tt, J=6.9, 23.9, 1H), 3.19-3.25 (m, 2H), 3.29 (dd, J=5.2, 7.6, 1H), 4.58-4.63 (m, 8H), 5.25 (dq, J=1.3, 10.3, 4H), 5.38 (dq, J=1.4, 17.1, 4H), 5.90-6.00 (m, 4H), 6.14 (bd, J=4.9, 1H): 31P (162 MHz, CDCl3) δ 24.67 (s, 2P).
後処理
- washwas washed with water and brine
- dry with materialthen dried over Na2SO4
- concentrationconcentrated in vacuo
- customThe crude material was purified by silica gel chromatography (methanol in ethyl acetate, 5% over 5 column volumes
出典と根拠
- ORDレコード
- ord-9ace8feb681144c797b9b24e1829a87f
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524691B2
関連ノート
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