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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-azidomethyl-5-methyl-2-phenyl-1H-imidazole → C-(5-methyl-2-phenyl-1H-imidazol-4-yl)-methylamine

HRID 982846
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HRID 982846 반응식
[N:1]([CH2:4][C:5]1[N:6]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[NH:8][C:9]=1[CH3:10])=[N+]=[N-]>C(O)C.[Pd]>[CH3:10][C:9]1[NH:8][C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:6][C:5]=1[CH2:4][NH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 225633704-azidomethyl-5-methyl-2-phenyl-1H-imidazole

생성물 1

HCID 22563473C-(5-methyl-2-phenyl-1H-imidazol-4-yl)-methylamine수율 98.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To solution of 4-azidomethyl-5-methyl-2-phenyl-1H-imidazole (1.22 g) in ethanol (50 ml) was added 10% Pd/C (0.10 g). The reaction mixture was hydrogenated at room temperature and 1.1 bar for 30 minutes, the catalyst was filtered off over a pad of celite. The filtrate was evaporated to dryness under high vacuum to obtain C-(5-methyl-2-phenyl-1H-imidazol-4-yl)-methylamine (1.06 g) as a light yellow foam which was sufficiently pure to be used directly in the next step.

후처리

  1. customwas hydrogenated at room temperature
  2. filtrationthe catalyst was filtered off over a pad of celite
  3. customThe filtrate was evaporated to dryness under high vacuum

출처 및 근거

ORD 기록
ord-c7bdcad7f7af4e7888728e99ebd7b87a
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06861440B2

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