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(Z)-1-Ethoxy-2-(tributylstannyl)ethene → 1-[4-(5H,11H-pyrrolo[2,1-c][1,4]benzodiazepine-10-carbonyl)-3-chlorophenyl]-ethanone

HRID 2307395
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HRID 2307395 반응식
C([Sn](CCCC)(CCCC)[CH:6]=[CH:7][O:8]CC)CCC.Br[C:20]1[CH:25]=[CH:24][C:23]([C:26]([N:28]2[C:34]3[CH:35]=[CH:36][CH:37]=[CH:38][C:33]=3[CH2:32][N:31]3[CH:39]=[CH:40][CH:41]=[C:30]3[CH2:29]2)=[O:27])=[C:22]([Cl:42])[CH:21]=1>C1(C)C=CC=CC=1>[CH:41]1[CH:40]=[CH:39][N:31]2[CH2:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[N:28]([C:26]([C:23]3[CH:24]=[CH:25][C:20]([C:7](=[O:8])[CH3:6])=[CH:21][C:22]=3[Cl:42])=[O:27])[CH2:29][C:30]=12
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참가 물질

4

반응물 2

HCID 2763294(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 9909050HCID 9909050, 화합물

생성물 1

HCID 99509821-[4-(5H,11H-pyrrolo[2,1-c][1,4]benzodiazepine-10-carbonyl)-3-chlorophenyl]-ethanone수율 26.6%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Tributyl(ethoxyvinyl)tin (1.17 g) was added to a solution of (4-bromo-2-chlorophenyl)-(5H,11H-pyrrolo[2,1-c][1,4]benzodiazepin-10-yl)-methanone (1.24 g) in toluene (10 ml). The resultant solution was purged with nitrogen for 10 minutes, then bis(triphenylphosphine)palladium (II) chloride (0.11 g) was added. The reaction mixture was heated to reflux for 24 hours. The solution was cooled to room temperature and 5% aqueous hydrochloric acid (10 ml) was added. After stirring for one hour, the mixture was filtered through a pad of diatomaceous. Diethyl ether (5 ml) was added to the filtrate, and the resulting mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered, and evaporated in vacuo to yield a brown glass. Purification by flash chromatography on silica gel eluting with hexane-ethyl acetate (1:1) resulted in a white solid (0.30 g), MS, m/z: 364 (M)+.

후처리

  1. customThe resultant solution was purged with nitrogen for 10 minutes
  2. additionbis(triphenylphosphine)palladium (II) chloride (0.11 g) was added
  3. temperatureThe reaction mixture was heated
  4. temperatureto reflux for 24 hours
  5. addition5% aqueous hydrochloric acid (10 ml) was added
  6. filtrationthe mixture was filtered through a pad of diatomaceous
  7. additionDiethyl ether (5 ml) was added to the filtrate
  8. extractionthe resulting mixture was extracted with ethyl acetate
  9. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  10. filtrationfiltered
  11. customevaporated in vacuo
  12. customto yield a brown glass
  13. customPurification by flash chromatography on silica gel eluting with hexane-ethyl acetate (1:1)

출처 및 근거

ORD 기록
ord-26f6343d9c4f42ff86edfbc7a833affb
출처 데이터셋
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06831079B1

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