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Trifluoroacetic acid → [(2S)-2-Methyl-1-piperazinyl]phenylmethanone

HRID 1689959
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HRID 1689959 반응식
[C:1]([N:9]1[CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11][C@@H:10]1[CH3:22])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.FC(F)(F)C(O)=O>ClCCl>[CH3:22][C@H:10]1[CH2:11][NH:12][CH2:13][CH2:14][N:9]1[C:1]([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 57581556HCID 57581556, 화합물

생성물 1

HCID 57581475[(2S)-2-Methyl-1-piperazinyl]phenylmethanone

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(S)-tert-butyl 4-benzoyl-3-methylpiperazine-1-carboxylate (8.16 g, 26.8 mmol) was dissolved in dichloromethane (200 mL). Trifluoroacetic acid (20.7 ml) was added and the reaction was stirred at rt for 1.5 hours. The reaction was quenched into saturated K2CO3 (30 mL) and neutralized by the portion-wise addition of solid NaHCO3. The layers were separated and extracted twice with dichloromethane. The combined organics were dried (MgSO4) and evaporated to give a yellow oil. MS (M+H)+=205.3.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe reaction was quenched into saturated K2CO3 (30 mL)
  2. additionneutralized by the portion-wise addition of solid NaHCO3
  3. customThe layers were separated
  4. extractionextracted twice with dichloromethane
  5. dry with materialThe combined organics were dried (MgSO4)
  6. customevaporated
  7. customto give a yellow oil

출처 및 근거

ORD 기록
ord-cb30c2f8c58b427298c22302d42b8756
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153633B2

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