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Toluene → 3-((1-(3-Chloro-4-morpholinophenyl)-4-methyl-6-oxo-1,6-dihydro pyrimidin-2-yl)methoxy)benzonitrile

HRID 56284
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HRID 56284 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([NH:14][C:15](=[O:20])[CH2:16][C:17](=O)[CH3:18])[CH:5]=[CH:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1.[C:21]([C:23]1[CH:24]=[C:25]([CH:31]=[CH:32][CH:33]=1)[O:26][CH2:27][C:28]([NH2:30])=O)#[N:22].C1(C)C=CC=CC=1.[NH4+].[Cl-]>C1(C)C(C)=CC=CC=1.C([O-])(C)C.C([O-])(C)C.C([O-])(C)C.C([O-])(C)C.[Ti+4]>[Cl:1][C:2]1[CH:3]=[C:4]([N:14]2[C:15](=[O:20])[CH:16]=[C:17]([CH3:18])[N:30]=[C:28]2[CH2:27][O:26][C:25]2[CH:24]=[C:23]([CH:33]=[CH:32][CH:31]=2)[C:21]#[N:22])[CH:5]=[CH:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1
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참가 물질

7

반응물 4

HCID 1140TolueneHCID 25517Ammonium ChlorideHCID 246951822-(3-Cyanophenoxy)acetamideHCID 90022603N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide

생성물 1

HCID 900516983-((1-(3-Chloro-4-morpholinophenyl)-4-methyl-6-oxo-1,6-dihydro pyrimidin-2-yl)methoxy)benzonitrile수율 59%

시약·촉매·용매 2

HCID 11026
Titanium isopropoxide
촉매
HCID 7237O-Xylene용매

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온도
165 °C

실험 절차

A mixture of N-(3-chloro-4-morpholinophenyl)-3-oxobutanamide (0.59 g, 2.00 mmol), 2-(3-cyanophenoxy)acetamide (0.71 g, 4.03 mmol) and titanium tetraisopropanolate (4.8 mL) in xylene (20 mL) was stirred at 165° C. for 24 h. The mixture was cooled to rt and 30 mL of toluene and 40 mL of saturated NH4Cl aqueous solution were added. The resulting mixture was stirred at rt overnight and filtered and the filtrate was extracted with DCM (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (0.51 g, 59%). The compound was characterized by the following spectroscopic data:

후처리

  1. temperatureThe mixture was cooled to rt
  2. stirringThe resulting mixture was stirred at rt overnight
  3. filtrationfiltered
  4. extractionthe filtrate was extracted with DCM (50 mL×3)
  5. dry with materialThe combined organic layers were dried over anhydrous Na2SO4
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1)

출처 및 근거

ORD 기록
ord-ef2f69ccb96546ffaf4a36f58f764d11
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434695B2

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