反応式
Cl[C:2]1[C:3]2[CH:10]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([CH2:17][OH:18])=[CH:13][CH:12]=3)[NH:8][C:4]=2[N:5]=[CH:6][N:7]=1.[CH3:19][O:20][C:21]1[CH:26]=[C:25]([NH2:27])[CH:24]=[CH:23][N:22]=1.COC1C=C([N+]([O-])=O)C=C[N+]=1[O-].C(Cl)(Cl)Cl>CO.C1COCC1.O.[Ni].CCOC(C)=O>[CH3:19][O:20][C:21]1[CH:26]=[C:25]([NH:27][C:2]2[C:3]3[CH:10]=[C:9]([C:11]4[CH:16]=[CH:15][C:14]([CH2:17][OH:18])=[CH:13][CH:12]=4)[NH:8][C:4]=3[N:5]=[CH:6][N:7]=2)[CH:24]=[CH:23][N:22]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 4
反応条件
- 温度
- 70 °C
実験手順
To 4.16 g (16 mMol) of [4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-phenyl]-methanol (see Step 108.3) and 1.99 g (16 mMol) of 2-methoxy-pyridin-4-ylamine [see Rec. Trav. Chim. (1955) 74, 1160; prepared from 2-methoxy-4-nitro-pyridine-1-oxide by hydrogenation in the presence of Raney-Nickel in methanol/THF] in 90 ml degassed DMF under N2-atmosphere, 996 mg of R(+)-BINAP [R(+)-2,2′-bis-(diphenylphosphino)-1,1′-binaphthalin); 1.6 mMol], 414 mg Pd2(dba)3.CHCl3 [tris(dibenzylideneacetone)dipalladium (0) chloroform complex; 0.40 mMol] and 3.08 g (32 mMol) of sodium-tert-butylate are subsequently added. The red solution is stirred at 70° C. over night and then poured into a mixture of 0.5 l of EtOAc and 1 l buffer (7.8 g of NaH2PO4.2H2O, 5 g of Na2HPO4.2H2O in 1 l H2O). After stirring for 1 h, the title compound is filtered off and washed with water and EtOAc; HPLC (conditions see Examples 67-78) tR=8.2 min; MS-ES+: (M+H)+=348.
後処理
- customdegassed DMF under N2-atmosphere
- stirringAfter stirring for 1 h
- filtrationthe title compound is filtered off
- washwashed with water and EtOAc
出典と根拠
- ORDレコード
- ord-da8979d0b6624302a4e7b58afa765c03
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07390805B2
関連ノート
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