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1,1'-Carbonyldiimidazole → 3-(4-Fluorophenyl)-5-[2-(2-chlorophenyl)propionylamino]-4-[4-pyrimidinyl]isoxazole

HRID 547451
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HRID 547451 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]([CH3:12])[C:9]([OH:11])=O.C1N=CN(C(N2C=NC=C2)=O)C=1.C1CCN2C(=NCCC2)CC1.[NH2:36][C:37]1[O:41][N:40]=[C:39]([C:42]2[CH:47]=[CH:46][C:45]([F:48])=[CH:44][CH:43]=2)[C:38]=1[C:49]1[CH:54]=[CH:53][N:52]=[CH:51][N:50]=1>C1COCC1>[F:48][C:45]1[CH:46]=[CH:47][C:42]([C:39]2[C:38]([C:49]3[CH:54]=[CH:53][N:52]=[CH:51][N:50]=3)=[C:37]([NH:36][C:9](=[O:11])[CH:8]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[Cl:1])[CH3:12])[O:41][N:40]=2)=[CH:43][CH:44]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 682631,1'-CarbonyldiimidazoleHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 126365742-(2-Chlorophenyl)propanoic acidHCID 574677255-Amino-3-(4-fluorophenyl)-4-(4-pyrimidinyl)isoxazole

생성물 1

HCID 671981653-(4-Fluorophenyl)-5-[2-(2-chlorophenyl)propionylamino]-4-[4-pyrimidinyl]isoxazole수율 72%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

In 5 mL of THF, 0.144 g of 2-(2-chlorophenyl)propionic acid and 0.126 g of CDI were dissolved and stirred at room temperature for an hour. Then 5 mL of THF solution containing 0.237 g of DBU and 0.1 g of 5-amino-3 (4-fluorophenyl)-4-4-pyrimidinyl isoxazole was added and stirred at room temperature for 3 hours. The solvent was distilled off from the reaction solution under reduced pressure, and water was added to the residue which was then extracted with ethyl acetate. The ethyl acetate extract was dried over anhydrous magnesium sulfate, removed of the solvent by distillation under reduced pressure, and the residue was purified on 20 g silica gel chromatography (eluent, chloroform:methanol=50:1). Washing the residue with ether, 0.118 g (yield: 72%) of the title compound was obtained.

후처리

  1. additionwas added
  2. stirringstirred at room temperature for 3 hours
  3. distillationThe solvent was distilled off from the reaction solution under reduced pressure, and water
  4. additionwas added to the residue which
  5. extractionwas then extracted with ethyl acetate
  6. extractionThe ethyl acetate extract
  7. dry with materialwas dried over anhydrous magnesium sulfate
  8. customremoved of the solvent by distillation under reduced pressure
  9. customthe residue was purified on 20 g silica gel chromatography (eluent, chloroform:methanol=50:1)
  10. washWashing the residue with ether

출처 및 근거

ORD 기록
ord-1b57d0a242b54c36b1443860f70eb618
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07939536B2

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