Diisopropylethylamine → N-[[2-[(2R,6S)-2,6-dimethyl-4-morpholinyl]-5-(2,6-dimethyl-4-pyridinyl)-4-thiazolyl]methyl]-3-methyl-5-isoxazolecarboxamide
反応式
C[CH2:2][N:3](C(C)C)C(C)C.[CH3:10][C@H:11]1[O:16][C@@H:15]([CH3:17])[CH2:14][N:13]([C:18]2[S:19][C:20]([C:25]3[CH:30]=[C:29]([CH3:31])[N:28]=[C:27]([CH3:32])[CH:26]=3)=[C:21](NC)[N:22]=2)[CH2:12]1.[CH3:33][C:34]1[CH:38]=[C:37]([C:39](Cl)=[O:40])[O:36][N:35]=1>C(Cl)Cl>[CH3:10][C@H:11]1[O:16][C@@H:15]([CH3:17])[CH2:14][N:13]([C:18]2[S:19][C:20]([C:25]3[CH:26]=[C:27]([CH3:32])[N:28]=[C:29]([CH3:31])[CH:30]=3)=[C:21]([CH2:2][NH:3][C:39]([C:37]3[O:36][N:35]=[C:34]([CH3:33])[CH:38]=3)=[O:40])[N:22]=2)[CH2:12]1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 0 °C
実験手順
DIPEA (0.16 mL, 0.97 mmol) was added to a solution of Intermediate 5 (150 mg, 0.45 mmol) in DCM (6 mL). The reaction mixture was cooled to 0° C. under nitrogen atmosphere. 3-Methylisoxazole-5-carbonyl chloride (79 mg, 0.54 mmol) was then added dropwise and stirring was continued for 1 h at room temperature. The reaction was washed with sodium bicarbonate and then twice with water. The organic layer was dried over a magnesium sulphate plug and evaporated. The residue was purified by preparative HPLC (RP Shandon Hyperprep C18 BDS—8 μm, 250 g, 5 cm; mobile phase (0.25% NH4HCO3 solution in water, CH3CN)), yielding 127 mg (64%) of Compound 4.
後処理
- washThe reaction was washed with sodium bicarbonate
- dry with materialThe organic layer was dried over a magnesium sulphate plug
- customevaporated
- customThe residue was purified by preparative HPLC (RP Shandon Hyperprep C18 BDS—8 μm, 250 g, 5 cm; mobile phase (0.25% NH4HCO3 solution in water, CH3CN))
出典と根拠
- ORDレコード
- ord-c37e071bf18a43a69220815a122cfa8e
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637510B2
反応ノート
読み込み中…