Potassium Carbonate → tert-butyl 1-(3-(4-chlorophenyl)-5,5,5-trifluoropent-1-yn-3-yl)-1H-indazol-4-ylcarbamate
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([N:16]2[C:24]3[C:19](=[C:20]([NH:25][C:26](=[O:32])[O:27][C:28]([CH3:31])([CH3:30])[CH3:29])[CH:21]=[CH:22][CH:23]=3)[CH:18]=[N:17]2)([CH2:11][C:12]([F:15])([F:14])[F:13])[CH:9]=O)=[CH:4][CH:3]=1.[C:33]([O-])([O-])=O.[K+].[K+].[N+](=C(P(=O)(OC)OC)C(=O)C)=[N-]>CO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([N:16]2[C:24]3[C:19](=[C:20]([NH:25][C:26](=[O:32])[O:27][C:28]([CH3:30])([CH3:31])[CH3:29])[CH:21]=[CH:22][CH:23]=3)[CH:18]=[N:17]2)([CH2:11][C:12]([F:13])([F:14])[F:15])[C:9]#[CH:33])=[CH:6][CH:7]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of the product of Step C (120 mg, 0.25 mmol) in methanol (5 mL) was added K2CO3 (69 mg, 0.5 mmol), dimethyl 1-diazo-2-oxopropylphosphonate (96 mg, 0.5 mmol). The mixture was stirred at room temperature for 2 h. After removing the organic solvent, the residue was added H2O (10 mL), extracted with ethyl acetate, and washed with brine (10 mL), dried over sodium sulfate, then filtered. The organic solvent was evaporated, and the residue was purified by silica gel chromatography (EA/PE=1:8) to obtain the title compound as colorless oil. LC/MS m/z=464.1[M+H]+.
後処理
- customAfter removing the organic solvent
- additionthe residue was added H2O (10 mL)
- extractionextracted with ethyl acetate
- washwashed with brine (10 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customThe organic solvent was evaporated
- customthe residue was purified by silica gel chromatography (EA/PE=1:8)
出典と根拠
- ORDレコード
- ord-a7f055e116514eb986ab429ecd44eb89
- 出典データセット
- uspto-grants-2015_01
- 特許番号
- US08933113B2
反応ノート
読み込み中…