Diisopropylethylamine → 5-Benzyloxy-2-(4,4-difluoro-piperidine-1-carbonyl)-pyrrolo[2,3-b]pyridine-1-carboxylic Acid tert-butyl Ester

HRID 1437698노트

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HRID 1437698 반응식
[C:1]([O:5][C:6]([N:8]1[C:12]2=[N:13][CH:14]=[C:15]([O:17][CH2:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:16]=[C:11]2[CH:10]=[C:9]1[C:25](O)=[O:26])=[O:7])([CH3:4])([CH3:3])[CH3:2].F[B-](F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.Cl.[F:51][C:52]1([F:58])[CH2:57][CH2:56][NH:55][CH2:54][CH2:53]1.C(N(CC)C(C)C)(C)C.C(=O)(O)[O-].[Na+]>CN(C=O)C>[C:1]([O:5][C:6]([N:8]1[C:12]2=[N:13][CH:14]=[C:15]([O:17][CH2:18][C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH:16]=[C:11]2[CH:10]=[C:9]1[C:25]([N:55]1[CH2:56][CH2:57][C:52]([F:58])([F:51])[CH2:53][CH2:54]1)=[O:26])=[O:7])([CH3:3])([CH3:4])[CH3:2]

참가 물질

7

실험 절차

To the solution of 2.3 g (6.2 mmol) 5-benzyloxy-pyrrolo[2,3-b]pyridine-1,2-dicarboxylic acid 1-tert-butyl ester (intermediate G), 2.5 g (7.8 mmol) O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate and 1.2 g (7.8 mmol) 4,4-difluoropiperidine hydrochloride in 30 ml DMF, 6.4 ml (4.8 g, 37.4 mmol) N,N-diisopropylethylamine were added. After 40 min. stirring at room temperature the clear solution was poured on saturated aqueous sodium bicarbonate solution and was extracted three times with ethyl acetate. The combined organic layers were washed three times with water and with brine, dried over magnesium sulfate, filtered and evaporated. The residue was re-crystallized from dichloromethane and n-heptane to give 2.8 g (95%) of the desired compound as a colorless solid.

후처리

  1. extractionwas extracted three times with ethyl acetate
  2. washThe combined organic layers were washed three times with water
  3. dry with materialwith brine, dried over magnesium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customThe residue was re-crystallized from dichloromethane and n-heptane

출처 및 근거

ORD 기록
ord-871f6431ed39457ebeb14cb1290fb053
출처 데이터셋
uspto-grants-2009_11
특허 번호
US07622466B2

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