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4-Azidomethyl-5-methyl-2-(4-trifluoromethyl-phenyl)-oxazole → C-[5-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-yl]-methylamine

HRID 860628
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인쇄 미리보기

반응식

HRID 860628 반응식
[N:1]([CH2:4][C:5]1[N:6]=[C:7]([C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=2)[O:8][C:9]=1[CH3:10])=[N+]=[N-].[H][H]>C(OCC)(=O)C.O=[Pt]=O>[CH3:10][C:9]1[O:8][C:7]([C:11]2[CH:12]=[CH:13][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:15][CH:16]=2)=[N:6][C:5]=1[CH2:4][NH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 587657284-Azidomethyl-5-methyl-2-(4-trifluoromethyl-phenyl)-oxazoleHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 58765787C-[5-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-yl]-methylamine수율 84.2%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 4-azidomethyl-5-methyl-2-(4-trifluoromethyl-phenyl)-oxazole (1.70 g) and PtO2 (0.106 g) in ethyl acetate (50 mL) at room temperature under 60 psi of hydrogen for 5 hrs, the reaction mixture is filtered through celite and filtrate is concentrated giving the title compound (1.3 g, 84.2% yield).

후처리

  1. filtrationthe reaction mixture is filtered through celite and filtrate
  2. concentrationis concentrated

출처 및 근거

ORD 기록
ord-744a3b20f6b44ed69c020b69c1e9456f
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07153878B2

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