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3-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(1-methylethenyl)benzonitrile → 3-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(1-methylethyl)benzonitrile

HRID 1874930
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HRID 1874930 반응식
[NH2:1][CH2:2][C:3]1[C:4]([F:22])=[C:5]([O:10][C:11]2[CH:12]=[C:13]([CH:16]=[C:17]([C:19]([CH3:21])=[CH2:20])[CH:18]=2)[C:14]#[N:15])[C:6]([Cl:9])=[CH:7][CH:8]=1>C(O)C.[Pt](=O)=O>[NH2:1][CH2:2][C:3]1[C:4]([F:22])=[C:5]([O:10][C:11]2[CH:12]=[C:13]([CH:16]=[C:17]([CH:19]([CH3:20])[CH3:21])[CH:18]=2)[C:14]#[N:15])[C:6]([Cl:9])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 684871183-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(1-methylethenyl)benzonitrile

생성물 1

HCID 684876543-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(1-methylethyl)benzonitrile

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(1-methylethenyl)benzonitrile (0.067 g, 0.212 mmol) dissolved in ethanol (10 mL) was treated with platinum(IV) oxide (0.050 g, 0.220 mmol) under hydrogen (1 atm) at 25° C. for 4 h. LC-MS indicates ˜90% conversion but multiple impurities are present. The reaction mixture was filtered through Celite and concentrated to give crude 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(1-methylethyl)benzonitrile as an amber oil which was used without further purification.

후처리

  1. filtrationThe reaction mixture was filtered through Celite
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1fdd3903687e4686a9d4dd72f6ee3d8f
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08304419B2

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