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Trifluoroacetic acid → 4-Methyl-1-(2-pyrazinyl)-4-piperidinamine

HRID 456746
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반응식

HRID 456746 반응식
[CH3:1][C:2]1([NH:14]C(=O)OC(C)(C)C)[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[N:12][CH:11]=[CH:10][N:9]=2)[CH2:4][CH2:3]1.FC(F)(F)C(O)=O>ClCCl>[CH3:1][C:2]1([NH2:14])[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[N:12][CH:11]=[CH:10][N:9]=2)[CH2:4][CH2:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 178608364-Tert-butoxycarbonylamino-4-methyl-1-(2-pyrazinyl)piperidine

생성물 1

HCID 178608804-Methyl-1-(2-pyrazinyl)-4-piperidinamine수율 84.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
20 °C

실험 절차

To a solution of tert-butyl [4-methyl-1-(2-pyrazinyl)-4-piperidinyl]carbamate obtained in Example 10-6 (508 mg) in dichloromethane (1 mL), was added trifluoroacetic acid (5 mL), and the mixture was stirred for 30 minutes at 20° C. The resulting mixture was evaporated in vacuo. The residue was neutralized with sodium hydrogencarbonate and extracted with chloroform three times. The organic layer was washed with brine, dried over MgSO4, and concentrated to give the title compound as a pale yellow solid (281 mg).

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후처리

  1. customThe resulting mixture was evaporated in vacuo
  2. extractionextracted with chloroform three times
  3. washThe organic layer was washed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-224af9d3ef924a779f61898dd733eeb4
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07186731B2

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