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1,1'-Carbonyldiimidazole → 1-Phenyl-5-phenoxy-3,4-dihydro-(1H)-quinazolin-2-one

HRID 1826835
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HRID 1826835 반응식
[O:1]([C:8]1[CH:15]=[CH:14][CH:13]=[C:12]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:9]=1[CH2:10][NH2:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:23](N1C=CN=C1)(N1C=CN=C1)=[O:24]>O1CCCC1>[C:17]1([N:16]2[C:12]3[C:9](=[C:8]([O:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)[CH:15]=[CH:14][CH:13]=3)[CH2:10][NH:11][C:23]2=[O:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 682631,1'-CarbonyldiimidazoleHCID 221362242-Phenoxy-6-(phenylamino)benzylamine

생성물 1

HCID 98617161-Phenyl-5-phenoxy-3,4-dihydro-(1H)-quinazolin-2-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

The product of example 1c above, 2-phenoxy-6-(phenylamino)benzyl amine, (0.165 g 0.57 mmol) was dissolved in dry tetrahydrofuran (5 mL) and stirred under argon at room temperature. 1,1′-Carbonyldiimidazole (0.120 g, 0.74 mmol) dissolved in dry tetrahydrofuran (2 mL) was added and the mixture stirred at room temperature. The solvent was evaporated in vacuo, to give the crude product which was flash chromatographed on silica gel eluted with 0–2% methanol in methylene chloride to give to the title compound as a white amorphous solid. mp 225–227° C.

후처리

  1. additionwas added
  2. stirringthe mixture stirred at room temperature
  3. customThe solvent was evaporated in vacuo
  4. customto give the crude product which
  5. customchromatographed on silica gel
  6. washeluted with 0–2% methanol in methylene chloride

출처 및 근거

ORD 기록
ord-f69158d16e4d45d1aab76335f5715877
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07053099B1

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