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HCID 66742608, 화합물 → 5-(4-Methylpiperazin-1-YL)pyrazin-2-amine

HRID 449634
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HRID 449634 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[N:12][C:11]([N+:14]([O-])=O)=[CH:10][N:9]=2)[CH2:4][CH2:3]1>CO.[Pd]>[CH3:1][N:2]1[CH2:3][CH2:4][N:5]([C:8]2[CH:13]=[N:12][C:11]([NH2:14])=[CH:10][N:9]=2)[CH2:6][CH2:7]1
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참가 물질

4

반응물 1

HCID 66742608HCID 66742608, 화합물

생성물 1

HCID 592999765-(4-Methylpiperazin-1-YL)pyrazin-2-amine수율 98.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

2-(4-methylpiperazin-1-yl)-5-nitropyrazine (328 mg, 1.47 mmol) was dissolved in MeOH (15 ml) at room temperature. Pd/C (10%) (50 mg) was added while the reaction mixture was stirred. The reaction mixture was placed under a H2 balloon and stirred at rt for 1.5 hrs. The reaction mixture was filtered through celite and washed with MeOH (30 mL). The filtrate was stripped and dried under vacuum after azeotroping with toluene twice to give a light brown gummy material (280 mg, yield 89%).

후처리

  1. stirringstirred at rt for 1.5 hrs
  2. filtrationThe reaction mixture was filtered through celite
  3. washwashed with MeOH (30 mL)
  4. customdried under vacuum
  5. customafter azeotroping with toluene twice

출처 및 근거

ORD 기록
ord-b591a05082434a8e9fc939d53a9b051d
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481540B2

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