Chloroform → {4-[4-(2-methoxy-pyridin-4-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-phenyl}-methanol
반응식
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]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 4
반응 조건
- 온도
- 70 °C
실험 절차
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+=348.
후처리
- customdegassed DMF under N2-atmosphere
- stirringAfter stirring for 1 h
- filtrationthe title compound is filtered off
- washwashed with water and EtOAc
출처 및 근거
- ORD 기록
- ord-9c5dcb906d704a2ca20d3d18e2ea65fc
- 출처 데이터셋
- uspto-grants-2008_01
- 특허 번호
- US07323469B2
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