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4-Aminophenol → 4-(5-(3,6-Dihydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline

HRID 410320
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HRID 410320 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.Cl[C:10]1[C:15]([C:16]2[CH2:17][CH2:18][O:19][CH2:20][CH:21]=2)=[CH:14][N:13]=[CH:12][N:11]=1.C(=O)([O-])[O-].[Cs+].[Cs+].CS(C)=O>O>[O:19]1[CH2:20][CH:21]=[C:16]([C:15]2[C:14]([O:8][C:5]3[CH:6]=[CH:7][C:2]([NH2:1])=[CH:3][CH:4]=3)=[N:13][CH:12]=[N:11][CH:10]=2)[CH2:17][CH2:18]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 4034-AminophenolHCID 679Dimethyl SulfoxideHCID 10796Cesium carbonateHCID 593268324-chloro-5-(3,6-dihydro-2H-pyran-4-yl)pyrimidine

생성물 1

HCID 593269884-(5-(3,6-Dihydro-2H-pyran-4-YL)pyrimidin-4-yloxy)aniline

시약·촉매·용매 1

HCID 962Water용매

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온도
100 °C

실험 절차

To a 150 mL sealable tube was added 4-aminophenol (388 mg, 3.56 mmol), 4-chloro-5-(3,6-dihydro-2H-pyran-4-yl)pyrimidine (700 mg, 3.56 mmol), and cesium carbonate (1218 mg, 3.74 mmol) with DMSO (23.700 ml). The vessel was sealed and heated to 100° C. for 2 h. The reaction mixture was cooled to room temperature and diluted with water before extracting with ethyl acetate. The combined organics were dried over sodium sulfate, filtered, and concentrated under reduced pressure to a dark brown oil that was used without purification. MS (ESI, pos. ion) m/z: 270.0 (M+1).

후처리

  1. customThe vessel was sealed
  2. temperatureThe reaction mixture was cooled to room temperature
  3. extractionbefore extracting with ethyl acetate
  4. dry with materialThe combined organics were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure to a dark brown oil that
  7. customwas used without purification

출처 및 근거

ORD 기록
ord-dd1912f6ced94d329a437b1064e320a5
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759532B2

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