Dichloromethane → (2S)-N-[3-(5H-dibenzo[a,d][7]annulen-5-ylidene)propyl]-N,4-dimethyl-2-(methylamino)pentanamide hydrochloride

HRID 2236005노트

반응식

HRID 2236005 반응식
FC(F)(F)C(O)=O.[CH:8]1[C:18]2[CH:17]=[CH:16][C:15]3[CH:19]=[CH:20][CH:21]=[CH:22][C:14]=3[C:13](=[CH:23][CH2:24][CH2:25][N:26]([CH3:43])[C:27]([C@@H:29]([N:34](C)[C:35](=O)OC(C)(C)C)[CH2:30][CH:31]([CH3:33])[CH3:32])=[O:28])[C:12]=2[CH:11]=[CH:10][CH:9]=1.[Cl:44]CCl>>[ClH:44].[CH:19]1[C:15]2[CH:16]=[CH:17][C:18]3[CH:8]=[CH:9][CH:10]=[CH:11][C:12]=3[C:13](=[CH:23][CH2:24][CH2:25][N:26]([CH3:43])[C:27](=[O:28])[C@@H:29]([NH:34][CH3:35])[CH2:30][CH:31]([CH3:33])[CH3:32])[C:14]=2[CH:22]=[CH:21][CH:20]=1

참가 물질

4

실험 절차

5 ml of dichloromethane and 2.5 ml of trifluoroacetic acid were added to 169 mg (0.35 mmol) of t-butyl (1S)-1-{[[3-(5H-dibenzo[a,d][7]annulen-5-ylidene)propyl] (methyl) amino]carbonyl}-3-methylbutyl(methyl)carbamate, and they were stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure. 1 N aqueous sodium hydroxide solution was added thereto to make it basic. After extracting with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was dissolved in 5 ml of 1,4-dioxane. 4 N hydrochloric acid/1,4-dioxane solution was added to the obtained solution. The resultant mixture was concentrated under reduced pressure to obtain the title compound.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. addition1 N aqueous sodium hydroxide solution was added
  3. extractionAfter extracting with ethyl acetate
  4. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. dissolutionThe residue was dissolved in 5 ml of 1,4-dioxane
  7. addition4 N hydrochloric acid/1,4-dioxane solution was added to the obtained solution
  8. concentrationThe resultant mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-14e8fccb0be946c58a4daf2e44ce9555
출처 데이터셋
uspto-grants-2010_05
특허 번호
US07713957B2

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