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4-Oxobutanoic acid → Ethyl 4-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-butanoate

HRID 599733
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HRID 599733 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH:14]2[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O=[CH:21][CH2:22][CH2:23][C:24]([OH:26])=[O:25].[BH-](OC(C)=O)(OC(C)=O)O[C:29]([CH3:31])=O.[Na+].C([O-])([O-])=O.[K+].[K+]>C1COCC1.CC(O)=O>[CH2:1]([N:8]1[CH2:9][CH2:10][N:11]([CH:14]2[CH2:19][CH2:18][N:17]([CH2:21][CH2:22][CH2:23][C:24]([O:26][CH2:29][CH3:31])=[O:25])[CH2:16][CH2:15]2)[CH2:12][CH2:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 11124-Oxobutanoic acidHCID 11430Potassium CarbonateHCID 36792751-Benzyl-4-piperidin-4-yl-piperazineHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 66941713Ethyl 4-[4-(4-benzyl-piperazin-1-yl)-piperidin-1-yl]-butanoate

시약·촉매·용매 2

HCID 176
Acetic Acid
용매
HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 3.11 g (12.0 mmol) 1-benzyl-4-piperidin-4-yl-piperazine and 7.5 mL (12.0 mmol, 15% in water) 4-oxo-butanoic acid in 70 mL THF was adjusted to pH 5 with AcOH and stirred for 1 h at RT. While cooling with ice, 5.35 g (24.0 mmol) NaBH(OAc)3 were added batchwise and the mixture was then stirred overnight at RT. 80 mL of 30% K2CO3 solution were added dropwise to the reaction mixture within 15 min and after the addition had ended this mixture was washed twice with EtOAc. The aqueous phase was evaporated down by half i.vac., neutralised with 1 M KHSO4 solution, the precipitate formed was suction filtered, the filtrate was washed again with EtOAc and the aqueous phase was concentrated by evaporation i.vac. 150 mL of ethanolic HCl (1.25 M) was added and the mixture was stirred overnight at RT. The mixture was evaporated down i.vac., the residue was taken up in a little 15% K2CO3 solution, extracted exhaustively with EtOAc and the combined organic phases were dried on Na2SO4. After the elimination of the desiccant and solvent the residue was reacted further without any purification.

후처리

  1. additionwere added batchwise
  2. stirringthe mixture was then stirred overnight at RT
  3. additionafter the addition
  4. washwas washed twice with EtOAc
  5. customThe aqueous phase was evaporated down by half i.vac
  6. customthe precipitate formed
  7. filtrationfiltered
  8. washthe filtrate was washed again with EtOAc
  9. concentrationthe aqueous phase was concentrated by evaporation i.vac
  10. addition150 mL of ethanolic HCl (1.25 M) was added
  11. stirringthe mixture was stirred overnight at RT
  12. customThe mixture was evaporated down i.vac
  13. extractionextracted exhaustively with EtOAc
  14. customthe combined organic phases were dried on Na2SO4
  15. customAfter the elimination of the desiccant and solvent the residue was reacted further without any purification

출처 및 근거

ORD 기록
ord-31009ec7d3fb4babb4648ead23cb0c09
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07897603B2

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