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1,1'-Thiocarbonyldi-2(1H)-pyridone → N-(2,4-Difluoro-3-isothiocyanato-benzyl)-2,2-dimethyl-propionamide

HRID 1258696
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HRID 1258696 반응식
[C:1](N1C=CC=CC1=O)(N1C=CC=CC1=O)=[S:2].[NH2:17][C:18]1[C:19]([F:33])=[C:20]([CH:29]=[CH:30][C:31]=1[F:32])[CH2:21][NH:22][C:23](=[O:28])[C:24]([CH3:27])([CH3:26])[CH3:25]>O1CCOCC1>[F:33][C:19]1[C:18]([N:17]=[C:1]=[S:2])=[C:31]([F:32])[CH:30]=[CH:29][C:20]=1[CH2:21][NH:22][C:23](=[O:28])[C:24]([CH3:27])([CH3:26])[CH3:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8531621,1'-Thiocarbonyldi-2(1H)-pyridoneHCID 56839977N-(3-amino-2,4-difluoro-benzyl)-2,2-dimethyl-propionamide

생성물 1

HCID 56840193N-(2,4-Difluoro-3-isothiocyanato-benzyl)-2,2-dimethyl-propionamide

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

1,1′-Thiocarbonyldi-2-pyridone (546 mg, 2.35 mmol) was added to a mixture of N-(3-amino-2,4-difluoro-benzyl)-2,2-dimethyl-propionamide (570 mg, 2.35 mmol) and dioxane (20 mL) and stirred at reflux overnight. The mixture was concentrated, diluted with DCM and filtered over silica gel. The filtrate was concentrated to give the sub-title compound.

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후처리

  1. temperatureat reflux overnight
  2. concentrationThe mixture was concentrated
  3. additiondiluted with DCM
  4. filtrationfiltered over silica gel
  5. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-83a84f38d0a942d9ad640438519713a2
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08466186B2

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