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HCID 68762213, 화합물 → HCID 68761562, 화합물

HRID 79573
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HRID 79573 반응식
C([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][N:17]=[C:16]3[NH:20][CH:21]=[C:22]([NH:23][C:24](=[O:28])[CH2:25][CH2:26][CH3:27])[C:15]=23)[CH2:10][CH2:9]1)C1C=CC=CC=1>CO.Cl.[Pd]>[N:11]1([C:14]2[CH:19]=[CH:18][N:17]=[C:16]3[NH:20][CH:21]=[C:22]([NH:23][C:24](=[O:28])[CH2:25][CH2:26][CH3:27])[C:15]=23)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 68762213HCID 68762213, 화합물

생성물 1

HCID 68761562HCID 68761562, 화합물수율 93.8%

시약·촉매·용매 3

HCID 313Hydrochloric Acid촉매HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

N-(4-(4-Benzylpiperazin-1-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl)butyramide (0.070 g, 0.19 mmol) was dissolved in MeOH (1 mL). Pd/C (0.0197 g, 0.0185 mmol) was then added, followed by the addition of 3 drops of concentrated HCl. The reaction was then placed under a H2 balloon for 18 hours. The reaction was then filtered, washed with MeOH, and concentrated to give the crude product N-(4-(piperazin-1-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl)butyramide (0.050 g, 93.8% yield).

후처리

  1. customfor 18 hours
  2. filtrationThe reaction was then filtered
  3. washwashed with MeOH
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-521b0c305ac943fc9b03524b907a1f7b
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841304B2

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