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Trifluoroacetic acid → 4-[2-(2-Methoxy-phenyl)-ethyl]-pyridin-2-ylamine

HRID 1023448
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반응식

HRID 1023448 반응식
C(OC(=O)[NH:7][C:8]1[CH:13]=[C:12]([CH2:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[O:22][CH3:23])[CH:11]=[CH:10][N:9]=1)(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[CH3:23][O:22][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[CH2:15][CH2:14][C:12]1[CH:11]=[CH:10][N:9]=[C:8]([NH2:7])[CH:13]=1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 69085786{4-[2-(2-Methoxy-phenyl)-ethyl]-pyridin-2-yl}-carbamic acid tert-butyl ester

생성물 1

HCID 641288554-[2-(2-Methoxy-phenyl)-ethyl]-pyridin-2-ylamine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of {4-[2-(2-methoxy-phenyl)-ethyl]-pyridin-2-yl}-carbamic acid tert-butyl ester (143 mg, 0.435 mmol) in dry CH2Cl2 (3 mL) is treated with trifluoroacetic acid (1.0 mL, 13 mmol), and stirred at room temperature. After 18 hours, the reaction mixture is concentrated and the residue is dissolved in CH2Cl2 (10 mL), extracted with saturated aqueous NaHCO3 (10 mL) and brine (10 mL), dried over MgSO4, filtered and concentrated to give the crude product which is used in the next reaction without purification.

후처리

  1. concentrationthe reaction mixture is concentrated
  2. dissolutionthe residue is dissolved in CH2Cl2 (10 mL)
  3. extractionextracted with saturated aqueous NaHCO3 (10 mL) and brine (10 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-d5537c7eae8449ab833fe36ee990a14d
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722709B2

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