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1,1-Dimethylethyl 4-[[2-methoxy-5-(1-methylethyl)phenyl]methyl]-1-piperazinecarboxylate → 1-[[2-Methoxy-5-(1-methylethyl)phenyl]methyl]-piperazine

HRID 38291
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HRID 38291 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:11])[CH3:10])=[CH:5][C:4]=1[CH2:12][N:13]1[CH2:18][CH2:17][N:16](C(OC(C)(C)C)=O)[CH2:15][CH2:14]1>C(O)(C(F)(F)F)=O.ClCCl>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:11])[CH3:10])=[CH:5][C:4]=1[CH2:12][N:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1
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참가 물질

4

반응물 1

HCID 671315531,1-Dimethylethyl 4-[[2-methoxy-5-(1-methylethyl)phenyl]methyl]-1-piperazinecarboxylate

생성물 1

HCID 39064451-[[2-Methoxy-5-(1-methylethyl)phenyl]methyl]-piperazine수율 126.8%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of the product from step (a) (1.98 g) in TFA (4 ml) and dichloromethane (2 ml) was stirred for 2 h. The solvent was removed in vacuo and the residue azeotroped with toluene. Aq. potassium carbonate was added and the mixture was extracted with dichloromethane. The organic extracts were dried (MgSO4) and evaporated in vacuo to give the sub-title compound (1.79 g).

후처리

  1. customThe solvent was removed in vacuo
  2. customthe residue azeotroped with toluene
  3. additionAq. potassium carbonate was added
  4. extractionthe mixture was extracted with dichloromethane
  5. dry with materialThe organic extracts were dried (MgSO4)
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-cb22901767bf426b84b966e953a02f2d
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524715B2

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