Diisopropylethylamine → N-[4-(2-Amino-5-bromopyridin-3-yl)phenyl]-1-(2-fluoroethyl)-5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxamide

HRID 1428107노트

반응식

HRID 1428107 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]=1

참가 물질

7

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

  1. stirringThe mixture was stirred for six hours
  2. extractionAfter extraction with ethyl acetate
  3. washthe organic layer was washed with brine
  4. dry with materialdried over sodium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. 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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