反応式
Br[C:2]1[CH:28]=[CH:27][C:5]2[C@@H:6]3[C@H:19]([NH:20][C:21](=[O:26])[C:22]([F:25])([F:24])[F:23])[CH2:18][CH2:17][CH2:16][N:7]3[C:8]3[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:9]=3[O:10][C:4]=2[CH:3]=1.[Cl-].[CH3:30][Zn+].[NH4+].[Cl-]>C1COCC1.[CH-]1C=CC=C1.[CH-]1C=CC=C1.[Fe+2].Cl[Pd]Cl>[Cl:15][C:13]1[CH:12]=[CH:11][C:9]2[O:10][C:4]3[CH:3]=[C:2]([CH3:30])[CH:28]=[CH:27][C:5]=3[C@@H:6]3[C@H:19]([NH:20][C:21](=[O:26])[C:22]([F:23])([F:25])[F:24])[CH2:18][CH2:17][CH2:16][N:7]3[C:8]=2[CH:14]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 60 °C
実験手順
To a solution of trans-N-(12-bromo-7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido-[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide (80 mg, 0.17 mmol) in THF (2 mL) was added ferrocene PdCl2 (5 mg, 7 μmol), and the reaction mixture was stirred for 5 min. Methylzinc chloride was added dropwise whereafter the reaction mixture was heated to 60° C. and stirred overnight at 60° C. The mixture was poured into sat (aq) NH4Cl and extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried (Na2SO4) and evaporated. After purification on silica and with HPLC the title compound was obtained (13.2 mg, 19%). Data: 1H-NMR (400 MHz, DMSO) 1.60-1.85 (m, 3H), 2.0 (m, 1H), 2.23 (s, 3H), 3.11 (td, J=2.8, 13.2, 1H), 3.85 (d, J=14, 1H), 4.10 (d, J=10, 1H), 4.40 (m, 1H), 6.69-7.10 (6 ArH), 9.16 (d, J=10, 1H).
後処理
- stirringstirred overnight at 60° C
- additionThe mixture was poured
- extractionextracted with ethyl acetate (3×)
- washThe combined organic layers were washed with brine
- dry with materialdried (Na2SO4)
- customevaporated
- customAfter purification on silica
出典と根拠
- ORDレコード
- ord-74de55984cef41bc8c4b69e2239e6d49
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07737136B2
関連ノート
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