Triethylamine → N-(7-chloro-2,3-dihydro-1H-inden-1-yl)-N-cyclopropyl-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide
反応式
[F:1][C:2]1[N:6]([CH3:7])[N:5]=[C:4]([CH3:8])[C:3]=1[C:9](Cl)=[O:10].[Cl:12][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]2[C:21]=1[CH:20]([NH:22][CH:23]1[CH2:25][CH2:24]1)[CH2:19][CH2:18]2.C(N(CC)CC)C.CCCCCCC.C(OCC)(=O)C>O1CCCC1>[Cl:12][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]2[C:21]=1[CH:20]([N:22]([CH:23]1[CH2:25][CH2:24]1)[C:9]([C:3]1[C:4]([CH3:8])=[N:5][N:6]([CH3:7])[C:2]=1[F:1])=[O:10])[CH2:19][CH2:18]2参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
At ambient temperature, a solution of 0.19 g (1.06 mmol) of 5-fluoro-1,3-dimethyl-1H-pyrazole-4-carbonyl chloride in 3 ml of tetrahydrofurane is added dropwise to a solution of 0.20 g (0.96 mmol) of 7-chloro-N-cyclopropyl-2,3-dihydro-1H-inden-1-amine and 0.15 ml triethylamine in 8 ml tetrahydrofurane. The reaction mixture is stirred for 3 hrs at reflux. The solvent is removed under vacuum and 10 ml of water are then added to the residue. The watery layer is extracted three times with ethyl acetate (3×20 ml); the combined organic layers are dried over magnesium sulphate and concentrated in vacuum. Column chromatography (gradient n-heptane/ethyl acetate) yields 0.26 mg (73% yield) of N-(7-chloro-2,3-dihydro-1H-inden-1-yl)-N-cyclopropyl-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide as an orange oil (M+1=348).
後処理
- temperatureat reflux
- customThe solvent is removed under vacuum and 10 ml of water
- additionare then added to the residue
- extractionThe watery layer is extracted three times with ethyl acetate (3×20 ml)
- dry with materialthe combined organic layers are dried over magnesium sulphate
- concentrationconcentrated in vacuum
出典と根拠
- ORDレコード
- ord-6b4b577df4a14373a1848a9b981a2962
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09102588B2
反応ノート
読み込み中…