Acetyl chloride → HCID 86701334、化合物
反応式
[F:1][C:2]1[CH:39]=[CH:38][C:5]([O:6][C@@H:7]2[C@@H:15]([O:16][C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=3)[C@H:14]([CH3:24])[O:13][C:12](=[O:25])[C@@H:11]([NH:26][C:27](=[O:37])[C:28]3[C:33]([OH:34])=[C:32]([O:35][CH3:36])[CH:31]=[CH:30][N:29]=3)[CH2:10][O:9][CH2:8]2)=[CH:4][CH:3]=1.[C:40](Cl)(=[O:42])[CH3:41]>C(Cl)Cl.CN(C1C=CN=CC=1)C>[C:40]([O:34][C:33]1[C:28]([C:27](=[O:37])[NH:26][C@H:11]2[CH2:10][O:9][CH2:8][C@H:7]([O:6][C:5]3[CH:4]=[CH:3][C:2]([F:1])=[CH:39][CH:38]=3)[C@@H:15]([O:16][C:17]3[CH:18]=[CH:19][C:20]([F:23])=[CH:21][CH:22]=3)[C@H:14]([CH3:24])[O:13][C:12]2=[O:25])=[N:29][CH:30]=[CH:31][C:32]=1[O:35][CH3:36])(=[O:42])[CH3:41]参加物
反応条件
- 温度
- 40 °C
実験手順
To a solution of N-((3S,7S,8S,9S)-7,8-bis(4-fluorophenoxy)-9-methyl-2-oxo-1,5-dioxonan-3-yl)-3-hydroxy-4-methoxypicolinamide (54 mg, 0.099 mmol) in DCM (0.5 mL) was added TEA (0.028 mL, 0.198 mmol), DMAP (6.1 mg, 0.050 mmol), and acetyl chloride (0.011 ml, 0.149 mmol). The reaction was warmed to 40° C. for and stirred for 14 h. The reaction was then concentrated and the crude residue purified by flash chromatography (SiO2, EtOAc/Hexanes) to give the title compound as a white foam (46.5 mg, 80%): IR (thin film) 3372, 2939, 1765, 1676 cm−1; 1H NMR (400 MHz, CDCl3) δ 8.78 (d, J=8.2 Hz, 1H), 8.37 (d, J=5.4 Hz, 1H), 7.03 (d, J=5.5 Hz, 1H), 6.98-6.86 (m, 6H), 6.74-6.61 (m, 2H), 5.33-5.24 (m, 1H), 5.14 (m, 1H), 4.36 (t, J=9.2 Hz, 1H), 4.30-4.22 (m, 1H), 4.10-3.99 (m, 2H), 3.92 (s, 3H), 3.92-3.87 (m, 1H), 3.79 (dd, J=11.2, 7.3 Hz, 1H), 2.40 (s, 3H), 1.48 (d, J=6.4 Hz, 3H); HRMS-FAB (m/z) [M+H]+ calcd for C29H28F2N2O9, 587.1836; found, 587.1838.
後処理
- concentrationThe reaction was then concentrated
- customthe crude residue purified by flash chromatography (SiO2, EtOAc/Hexanes)
出典と根拠
- ORDレコード
- ord-ecf5102c58284a6e982db6aed4cf8c97
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09144239B2
反応ノート
読み込み中…