Water → N-(2,6-diisopropylphenyl)-2-(2,2-dioxo-1-phenyl-2-thia-1,3-diazaspiro[4.5]dec-3-yl]acetamide

HRID 1894858

반응식

HRID 1894858 반응식
C(=O)([O-])[O-].[K+].[K+].[C:7]1([N:13]2[C:17]3([CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]3)[CH2:16][NH:15][S:14]2(=[O:24])=[O:23])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.Cl[CH2:26][C:27]([NH:29][C:30]1[C:35]([CH:36]([CH3:38])[CH3:37])=[CH:34][CH:33]=[CH:32][C:31]=1[CH:39]([CH3:41])[CH3:40])=[O:28].O>CN(C)C=O>[CH:39]([C:31]1[CH:32]=[CH:33][CH:34]=[C:35]([CH:36]([CH3:37])[CH3:38])[C:30]=1[NH:29][C:27](=[O:28])[CH2:26][N:15]1[CH2:16][C:17]2([CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)[N:13]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[S:14]1(=[O:23])=[O:24])([CH3:40])[CH3:41]

참가 물질

6

실험 절차

75 mg (0.54 mmol) of potassium carbonate are added to a solution of 130 mg (0.49 mmol) of 1-phenyl-2-thia-1,3-diazaspiro[4.5]decane-2,2-dioxide and 136 mg (0.54 mmol) of 2-chloro-N-(2,6-diisopropylphenyl)-acetamide in 30 ml of dimethylformamide. The reaction medium is stirred at room temperature for one night and then it is heated to reflux for 6 hours and at room temperature for 48 h. The medium is then poured into water and extracted with ethyl acetate. The organic phases are collected and washed with water. They are dried over sodium sulfate. The solvents are evaporated. The residue is chromatographed on silica gel (heptane/ethyl acetate 90/10). 125 mg of N-(2,6-diisopropylphenyl)-2-(2,2-dioxo-1-phenyl-2-thia-1,3-diazaspiro[4.5]dec-3-yl]acetamide are obtained in the form of a yellow oil. The product is triturated in dichloromethane and plenty of heptane. A solid is obtained. M.p. 140-2° C., yield=53%.

후처리

  1. temperatureit is heated
  2. temperatureto reflux for 6 hours and at room temperature for 48 h
  3. extractionextracted with ethyl acetate
  4. customThe organic phases are collected
  5. washwashed with water
  6. dry with materialThey are dried over sodium sulfate
  7. customThe solvents are evaporated
  8. customThe residue is chromatographed on silica gel (heptane/ethyl acetate 90/10)

출처 및 근거

ORD 기록
ord-79a5fb6caafa43a28a312bc2dfa1098e
출처 데이터셋
uspto-grants-2013_08
특허 번호
US08513307B2

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