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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 86720944, 화합물 → HCID 86720947, 화합물

HRID 524891
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HRID 524891 반응식
[CH:1]1([C:4]2[CH:5]=[N:6][CH:7]=[C:8]([N+:17]([O-])=O)[C:9]=2[N:10]2[CH2:15][CH2:14][N:13]([CH3:16])[CH2:12][CH2:11]2)[CH2:3][CH2:2]1.[H][H]>CO.[Pd]>[CH:1]1([C:4]2[C:9]([N:10]3[CH2:11][CH2:12][N:13]([CH3:16])[CH2:14][CH2:15]3)=[C:8]([NH2:17])[CH:7]=[N:6][CH:5]=2)[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 86720944HCID 86720944, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 86720947HCID 86720947, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 1-(3-cyclopropyl-5-nitro-4-pyridyl)-4-methyl-piperazine (220.4 mg, 0.8403 mmol) in methanol (25 mL) was added Pd on carbon (10%, Degussa, 6.387 mg, 0.006002 mmol). The reaction mixture was stirred at room temperature under a balloon of hydrogen, for 7 h. The reaction was filtered through a plug of Celite, washed with MeOH and the filtrate was concentrated in vacuo yielding 5-cyclopropyl-4-(4-methylpiperazin-1-yl)pyridin-3-amine as an orange residue. (194 mg, 99%).

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후처리

  1. filtrationThe reaction was filtered through a plug of Celite
  2. washwashed with MeOH
  3. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-c6939d2eba46452991f03d4d6a538d61
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09340546B2

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