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1,1'-Thiocarbonyldi-2(1H)-pyridone → 4-(4-Chlorophenyl)-6-isothiocyanatopyrimidine

HRID 1875958
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인쇄 미리보기

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HRID 1875958 반응식
[C:1](N1C=CC=CC1=O)(N1C=CC=CC1=O)=[S:2].[Cl:17][C:18]1[CH:23]=[CH:22][C:21]([C:24]2[N:29]=[CH:28][N:27]=[C:26]([NH2:30])[CH:25]=2)=[CH:20][CH:19]=1>>[Cl:17][C:18]1[CH:19]=[CH:20][C:21]([C:24]2[CH:25]=[C:26]([N:30]=[C:1]=[S:2])[N:27]=[CH:28][N:29]=2)=[CH:22][CH:23]=1
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참가 물질

3

반응물 2

HCID 8531621,1'-Thiocarbonyldi-2(1H)-pyridoneHCID 574765876-(4-Chlorophenyl)pyrimidin-4-amine

생성물 1

HCID 574765864-(4-Chlorophenyl)-6-isothiocyanatopyrimidine

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온도
60 °C

실험 절차

To a bright orange solution of 1,1′-thiocarbonyldipyridin-2(1H)-one (0.666 g, 2.87 mmol) dichloromethane/N,N-dimethylformamide at room temperature was added 6-(4-chlorophenyl)pyrimidin-4-amine (0.59 g, 2.87 mmol). The orange mixture was heated at 60° C. for 18 hours. The LC/MS showed the desired product peak as a major peak. The deep orange mixture was purified by silica gel chromatography (0-40% ethyl acetate-hexanes) to afford 4-(4-chlorophenyl)-6-isothiocyanatopyrimidine (0.322 g, 1.300 mmol, 45% yield) as an orange oil. LCMS R.T.=2.82; [M]+=248.03.

출처 및 근거

ORD 기록
ord-7d4ef6757de9456b9d88310f4a834c46
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08309577B2

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