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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 20228803, 화합물 → HCID 13728693, 화합물

HRID 1731303
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HRID 1731303 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH:8]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)/[CH:9]=[CH:10]/[N:11]([CH3:13])[CH3:12])[N:3]=1>C(O)C.[Pt]>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH:8]([C:14]2[CH:15]=[CH:16][C:17]([Cl:20])=[CH:18][CH:19]=2)[CH2:9][CH2:10][N:11]([CH3:13])[CH3:12])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 20228803HCID 20228803, 화합물

생성물 1

HCID 13728693HCID 13728693, 화합물

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 702Ethanol용매

실험 절차

A solution of E-2-bromo-6-(1-(4-chlorophenyl)-3-dimethylaminoallyl)pyridine (vide supra (2.0 g) in absolute ethanol (150 mL) was stirred under hydrogen with 10% Pt/C (0.86 g) for 48 hr. The reaction mixture was filtered through Celite and the reduction continued with fresh catalyst (0.67 g) for an additional 96 hr. Filtration through Celite and concentration under reduced pressure gave an oil which was chromatographed on silica gel (Waters Prep 500) with 3:1/methanol:methylene chloride. This provided 2-bromo-6-(1-(4-chlorophenyl)-3-dimethylaminopropyl)pyridine (0.66 g) as an oil:TLC Rf 0.22 (silica gel, methanol).

후처리

  1. filtrationThe reaction mixture was filtered through Celite
  2. filtrationFiltration
  3. concentrationthrough Celite and concentration under reduced pressure
  4. customgave an oil which
  5. customwas chromatographed on silica gel (Waters Prep 500) with 3:1/methanol

출처 및 근거

ORD 기록
ord-414a6e2c3c164e8a825ae9c8ea8f47fd
출처 데이터셋
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04621094

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