1,2-Dichloroethane → HCID 178438007, 화합물

HRID 734680노트

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HRID 734680 반응식
[F:1][C:2]([F:21])([F:20])[C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[CH2:14][C:13](=[O:15])[NH:12][C:11]([CH3:16])=[C:10]2[C:17]([OH:19])=O)=[CH:5][CH:4]=1.[NH2:22][C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[NH:28][N:27]=[C:26]2[CH2:32][CH3:33].C(Cl)CCl.CCN(CC)CC>CN(C=O)C.CCOC(C)=O.Cl>[CH2:32]([C:26]1[C:25]2[C:29](=[CH:30][CH:31]=[C:23]([NH:22][C:17]([C:10]3[CH:9]([C:6]4[CH:7]=[CH:8][C:3]([C:2]([F:20])([F:21])[F:1])=[CH:4][CH:5]=4)[CH2:14][C:13](=[O:15])[NH:12][C:11]=3[CH3:16])=[O:19])[CH:24]=2)[NH:28][N:27]=1)[CH3:33]

참가 물질

8

실험 절차

The product of Example 5, Step 2 (125 mg, 0.418 mmol, 1.00 equiv), 5-amino-3-ethylindazole (67 mg, 0.418 mmol, 1.0 equiv), and EDC (96 mg, 0.501 mmol, 1.20 equiv) were suspended in 1.25 mL DMF. Et3N (0.070 mL, 0.501 mmol, 1.2 equiv) was added and the solution was stirred at room temperature for 18 hrs. The reaction mixture was diluted with EtOAc and 1N HCl. The phases were separated, and the organic phase was washed twice with 1N HCl, once with satd. NaHCO3, and once with satd. NaCl. The organic phase was dried over Na2SO4, filtered, and concentrated en vacuo. The residue was triturated with EtOAc and CH2Cl2, filtered, and washed with CH2Cl2 to provide 32 mg (17%) of the title compound as an off white solid. MS (ES+) m/e 443 [M+H]+

후처리

  1. customThe phases were separated
  2. washthe organic phase was washed twice with 1N HCl, once with satd
  3. dry with materialThe organic phase was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated en vacuo
  6. customThe residue was triturated with EtOAc and CH2Cl2
  7. filtrationfiltered
  8. washwashed with CH2Cl2

출처 및 근거

ORD 기록
ord-35c926c432b64d19970292359d25dc7d
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07592357B2

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