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Methyl iodide → 1-(((Tert-butoxy)carbonyl)(methyl)amino)cyclopropane-1-carboxylic acid

HRID 1897671
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HRID 1897671 반응식
[C:1]([O:5][C:6]([NH:8][C:9]1([C:12]([OH:14])=[O:13])[CH2:11][CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].[CH3:17]I.[NH4+].[Cl-]>CN(C=O)C>[C:1]([O:5][C:6]([N:8]([CH3:17])[C:9]1([C:12]([OH:14])=[O:13])[CH2:11][CH2:10]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

6

반응물 4

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 6883961-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acid

생성물 1

HCID 143582621-(((Tert-butoxy)carbonyl)(methyl)amino)cyclopropane-1-carboxylic acid

시약·촉매·용매 1

HCID 6228Dimethylformamide
용매

실험 절차

To a solution of 1-(tert-butoxycarbonylamino)cyclopropanecarboxylic acid (201 mg, 1.0 mmol) in DMF (2 mL) was added NaH (120 mg, 3.0 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 10 min. before the addition of MeI (568 mg, 4.0 mmol). The mixture was then warmed up to room temperature and stirred for 2 hr. Saturated NH4Cl aqueous solution (20 mL) was added into the mixture, and the solution was extracted with EtOAc (3×10 mL). The combined organic layers were concentrated and the residue was dissolved in MeOH (3 ml) with NaOH (3 N, 1 mL). This mixture was stirred at 80° C. for 1 hr and cooled down to room temperature. The clear solution was purified directly on preparative RP-HPLC to provide 1-(tert-butoxycarbonyl(methyl)amino)cyclopropanecarboxylic acid. ESMS m/z 238.2 (M+Na+).

후처리

  1. extractionthe solution was extracted with EtOAc (3×10 mL)
  2. concentrationThe combined organic layers were concentrated
  3. dissolutionthe residue was dissolved in MeOH (3 ml) with NaOH (3 N, 1 mL)
  4. stirringThis mixture was stirred at 80° C. for 1 hr
  5. temperaturecooled down to room temperature
  6. customThe clear solution was purified directly on preparative RP-HPLC

출처 및 근거

ORD 기록
ord-ad64136a797d4f0c9eb782c802d9efd3
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08519129B2

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