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2-(Methylthio)pyrimidin-4-amine → 4-[3-(2,2,2-Trifluoroethyl)thioureido]-2-methylthiopyrimidine

HRID 1902289
노트
인쇄 미리보기

반응식

HRID 1902289 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([S:8][CH3:9])[N:3]=1.[F:10][C:11]([F:17])([F:16])[CH2:12][N:13]=[C:14]=[S:15]>C(#N)C>[F:10][C:11]([F:17])([F:16])[CH2:12][NH:13][C:14](=[S:15])[NH:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([S:8][CH3:9])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2592252-(Methylthio)pyrimidin-4-amineHCID 138837771,1,1-Trifluoro-2-isothiocyanatoethane

생성물 1

HCID 542472784-[3-(2,2,2-Trifluoroethyl)thioureido]-2-methylthiopyrimidine수율 51.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of 4-amino-2-methylthiopyrimidine (2.1 g.), 2,2,2-trifluoroethylisothiocyanate (2.8 g.) and acetonitrile (5 ml.) was stirred at 70° for 72 hours and then cooled, and the solid that crystallised was collected to give 4-[3-(2,2,2-trifluoroethyl)thioureido]-2-methylthiopyrimidine (2.15 g.) which was used without further purification.

후처리

  1. temperaturecooled
  2. customthe solid that crystallised
  3. customwas collected

출처 및 근거

ORD 기록
ord-a5a1411f1e3240088046ecbab9fa6024
출처 데이터셋
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04362728

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