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4-Bromobenzaldehyde → 4-[4-(4-Bromo-benzylamino)-2-nitro-phenylsulfanyl]-phenol

HRID 607212
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인쇄 미리보기

반응식

HRID 607212 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)=[C:4]([N+:16]([O-:18])=[O:17])[CH:3]=1.[Br:19][C:20]1[CH:27]=[CH:26][C:23]([CH:24]=O)=[CH:22][CH:21]=1>>[Br:19][C:20]1[CH:27]=[CH:26][C:23]([CH2:24][NH:1][C:2]2[CH:7]=[CH:6][C:5]([S:8][C:9]3[CH:10]=[CH:11][C:12]([OH:15])=[CH:13][CH:14]=3)=[C:4]([N+:16]([O-:18])=[O:17])[CH:3]=2)=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 707414-Bromobenzaldehyde2회HCID 668084374-(4-Amino-2-nitro-phenylsulfanyl)-phenol2회

생성물 1

HCID 668086074-[4-(4-Bromo-benzylamino)-2-nitro-phenylsulfanyl]-phenol수율 73%

실험 절차

A solution of the product from Example 84A and 4-Bromobenzaldehyde were reacted according to the procedure from Example 84B substituting 4-Bromobenzaldehyde for the product from Example 84A to provide the crude product which was purified by silica gel chromatography eluting with 2% methanol in methylene chloride to provide the title compound as a yellow solid (0.11 g, 73%).

후처리

  1. customto provide the crude product which
  2. customwas purified by silica gel chromatography
  • washeluting with 2% methanol in methylene chloride
  • 출처 및 근거

    ORD 기록
    ord-da4c614ce29040cd8f0dd71e72fce8b9
    출처 데이터셋
    uspto-grants-2011_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07915411B2

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