Acetamide → HCID 87192560, 화합물

HRID 2089007

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HRID 2089007 반응식
Cl[C:2]1[CH:7]=[C:6]([C:8]2[C:16]3[C:11](=[N:12][CH:13]=[CH:14][CH:15]=3)[N:10]([S:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)(=[O:19])=[O:18])[CH:9]=2)[CH:5]=[C:4]([Cl:26])[N:3]=1.[C:27]([NH2:30])(=[O:29])[CH3:28].C(=O)([O-])[O-].[Cs+].[Cs+].CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2>C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[Cl:26][C:4]1[N:3]=[C:2]([NH:30][C:27](=[O:29])[CH3:28])[CH:7]=[C:6]([C:8]2[C:16]3[C:11](=[N:12][CH:13]=[CH:14][CH:15]=3)[N:10]([S:17]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)(=[O:19])=[O:18])[CH:9]=2)[CH:5]=1

참가 물질

6

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온도
85 °C

실험 절차

A mixture of Example 7a (1.44 g, 3.57 mmol), acetamide (0.295 g, 4.99 mmol), cesium carbonate (1.743 g, 5.35 mmol), palladium (II) acetate (0.024 g, 0.107 mmol), and Xantphos (0.093 g, 0.161 mmol) was degassed and heated at 85° C. in a sealed vial for 6 hours. The reaction mixture was cooled and concentrated. The residue was treated with 20% brine and extracted with EtOAc (2×). The organic layers were dried, concentrated, and purified on a 40 g column using the ISCO Companion flash system eluting with CH2Cl2/EtOAc (90:10) to give 0.384 g of the title compound.

후처리

  1. temperatureThe reaction mixture was cooled
  2. concentrationconcentrated
  3. additionThe residue was treated with 20% brine
  4. extractionextracted with EtOAc (2×)
  5. customThe organic layers were dried
  6. concentrationconcentrated
  7. custompurified on a 40 g column
  8. washeluting with CH2Cl2/EtOAc (90:10)

출처 및 근거

ORD 기록
ord-9cf9dd06848645bfa34fc70ecf343d49
출처 데이터셋
uspto-grants-2013_05
특허 번호
US08435980B2

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