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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline → 5-Bromo-2-methyl-1,2,3,4-tetrahydroisoquinolin-8-amine

HRID 2237385
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인쇄 미리보기

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HRID 2237385 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:9]([N+:12]([O-])=O)=[C:8]2[C:3]=1[CH2:4][CH2:5][N:6]([CH3:15])[CH2:7]2>C(O)C.[Ni]>[Br:1][C:2]1[CH:11]=[CH:10][C:9]([NH2:12])=[C:8]2[C:3]=1[CH2:4][CH2:5][N:6]([CH3:15])[CH2:7]2
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참가 물질

4

반응물 1

HCID 100160105-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline

생성물 1

HCID 99919145-Bromo-2-methyl-1,2,3,4-tetrahydroisoquinolin-8-amine

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

To a solution of N-methyl-5-bromo-8-nitro-1,2,3,4-tetrahydroisoquinoline (III, 4.7 gm, 17.3 mmol) in ethanol (50 ml), Raney Nickel (solution in water, 1.5 g) was added. The reaction mixture was stirred at room temperature overnight under H2. The mixture was filtered through celite and solvent was removed under vacuum to give IV.

후처리

  1. filtrationThe mixture was filtered through celite and solvent
  2. customwas removed under vacuum

출처 및 근거

ORD 기록
ord-7c5288c394f14f128e7b45d721e163bd
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07718641B2

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