Methanol → HCID 59636036、化合物
反応式
[NH2:1][C@H:2]1[C@:12]2([CH3:14])[O:13][C@@:4]3([C@H:15]4[C@H:8]([N:9]([C:17]5[CH:24]=[CH:23][C:20]([C:21]#[N:22])=[C:19]([C:25]([F:28])([F:27])[F:26])[CH:18]=5)[C:10](=[O:16])[C@@H:11]24)[O:7][CH2:6][CH2:5]3)[CH2:3]1.[C:29](N1C=CN=C1)(N1C=CN=C1)=[O:30].[CH3:41][OH:42].C[O-].[Na+]>C1COCC1>[C:21]([C:20]1[CH:23]=[CH:24][C:17]([N:9]2[C@H:8]3[C@H:15]4[C@H:11]([C@@:12]5([CH3:14])[O:13][C@:4]4([CH2:5][CH2:6][O:7]3)[CH2:3][C@H:2]5[NH:1][C:29](=[O:30])[O:42][CH3:41])[C:10]2=[O:16])=[CH:18][C:19]=1[C:25]([F:26])([F:27])[F:28])#[N:22]参加物
6
実験手順
Example 13 (1.18 g, 3.0 mmol) in THF (10 mL) was added drop wise over 10 min to a solution of carbonyldiimidazole (1.5 g, 9.25 mmol) in THF (10 mL). The mixture was stirred for 30 min. Next, MeOH (20 mL) was added followed by the addition of NaOMe (0.162 g, 3 mmol). The reaction mixture was stirred for 5 min and then concentrated in vacuo. To the residue was added EtOAc and washed twice with 1M HCl and once with sat. NaHCO3 aq. The organic layer was dried over MgSO4, filtered, and then concentrated in vacuo. The residue was purified by silica gel chromatography on a 120 g ISCO column eluting with a gradient from 100% CH2Cl2 up to 6% MeOH/CH2Cl2. The product was collected, concentrated in vacuo, and dried to give 1.2 g of Example 14.
後処理
- customwise over 10 min
- stirringThe reaction mixture was stirred for 5 min
- concentrationconcentrated in vacuo
- additionTo the residue was added EtOAc
- washwashed twice with 1M HCl and once with sat. NaHCO3 aq. The organic layer
- dry with materialwas dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel chromatography on a 120 g ISCO column
- washeluting with a gradient from 100% CH2Cl2 up to 6% MeOH/CH2Cl2
- customThe product was collected
- concentrationconcentrated in vacuo
- customdried
出典と根拠
- ORDレコード
- ord-89682a52b5524e74afd33c936b9b00d9
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08067582B2
反応ノート
読み込み中…