Diisopropylamine → HCID 67407672、化合物
反応式
C(NC(C)C)(C)C.[Li]CCCC.[F:13][C:14]1[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=1.CON(C)[C:23]([CH:25]1[CH2:29][CH2:28][O:27][CH2:26]1)=[O:24]>C1COCC1>[F:13][C:14]1[CH:15]=[N:16][CH:17]=[CH:18][C:19]=1[C:23]([CH:25]1[CH2:29][CH2:28][O:27][CH2:26]1)=[O:24]参加物
実験手順
Diisopropylamine (605 μL, 4.30 mmol) was dissolved in THF (8 mL) and cooled to −78° C. nBuLi (1.72 mL, 2.5 M in hexanes, 4.30 mmol) was added and the resulting solution was stirred for 10 min, warmed to room temperature for 30 min and re-cooled to −78° C. 3-Fluoro-pyridine (370 μL, 4.30 mmol) was added drop-wise and the reaction mixture was stirred for 2 h. A solution of N-methoxy-N-methyloxolane-3-carboxamide (685 mg, 4.30 mmol) in THF (4.2 mL) was added drop-wise and the reaction mixture was warmed to room temperature and stirred for 15 min. The reaction mixture was quenched with sat aq NH4OAc (5 mL), diluted with EtOAc (50 mL), washed with water (2×25 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by normal phase column chromatography to give the title compound as a yellow gum (61.0 mg, 10%). LCMS (ES+): 196.0 (M+H)+.
後処理
- additionwas added
- temperaturere-cooled to −78° C
- stirringthe reaction mixture was stirred for 2 h
- temperaturethe reaction mixture was warmed to room temperature
- stirringstirred for 15 min
- customThe reaction mixture was quenched with sat aq NH4OAc (5 mL)
- additiondiluted with EtOAc (50 mL)
- washwashed with water (2×25 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customThe residue was purified by normal phase column chromatography
出典と根拠
- ORDレコード
- ord-f9ef90aad4c8444488d428b636413557
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09227967B2
反応ノート
読み込み中…