Diisopropylethylamine → N-[4-(2-Amino-5-bromopyridin-3-yl)phenyl]-1-(2-fluoroethyl)-5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxamide
반응식
CCN(C(C)C)C(C)C.[F:10][CH2:11][CH2:12][N:13]1[CH:18]=[C:17]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][CH:20]=2)[C:16](=[O:26])[C:15]([C:27]([OH:29])=O)=[CH:14]1.CCOC(C(C#N)=NOC(N1CCOCC1)=[N+](C)C)=O.F[P-](F)(F)(F)(F)F.[NH2:57][C:58]1[CH:63]=[CH:62][C:61]([C:64]2[C:65]([NH2:71])=[N:66][CH:67]=[C:68]([Br:70])[CH:69]=2)=[CH:60][CH:59]=1>CN(C=O)C.O>[NH2:71][C:65]1[C:64]([C:61]2[CH:60]=[CH:59][C:58]([NH:57][C:27]([C:15]3[C:16](=[O:26])[C:17]([C:19]4[CH:20]=[CH:21][C:22]([F:25])=[CH:23][CH:24]=4)=[CH:18][N:13]([CH2:12][CH2:11][F:10])[CH:14]=3)=[O:29])=[CH:63][CH:62]=2)=[CH:69][C:68]([Br:70])=[CH:67][N:66]=1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
DIPEA (114 μl) was added to a solution of the compound obtained in Step 2 of Example 8 (91 mg) and COMU (181 mg) in DMF (2.0 ml) at room temperature, and the mixture was stirred for 20 minutes. The compound obtained in Step 1 of Example 1 (95 mg) was added at room temperature. The mixture was stirred for six hours, followed by the addition of water. After extraction with ethyl acetate, the organic layer was washed with brine and then dried over sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography [chloroform:methanol=300:1->30:1 (v/v)] to give 139 mg of the title compound as a solid.
후처리
- stirringThe mixture was stirred for six hours
- extractionAfter extraction with ethyl acetate
- washthe organic layer was washed with brine
- dry with materialdried over sodium sulfate
- distillationThe solvent was distilled off under reduced pressure
- customthe residue was purified by silica gel column chromatography [chloroform:methanol=300:1->30:1 (v/v)]
출처 및 근거
- ORD 기록
- ord-ab457a7f35314049ad14cc0f5086d06e
- 출처 데이터셋
- uspto-grants-2015_01
- 특허 번호
- US08933103B2
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