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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Oxalyl chloride → Ammonia

HRID 419843
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HRID 419843 반응식
C(Cl)(=O)C(Cl)=O.[CH3:7][C:8]1[C:12]([CH2:13][CH2:14][C:15]([OH:17])=O)=[C:11]([CH3:18])[O:10][N:9]=1.[C:19]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])(=[O:22])[NH:20][NH2:21]>ClCCl.CN(C)C=O>[NH3:9].[CH3:7][C:8]1[C:12]([CH2:13][CH2:14][C:15]([NH:21][NH:20][C:19]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])=[O:17])=[C:11]([CH3:18])[O:10][N:9]=1
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참가 물질

7

반응물 3

HCID 65578Oxalyl chlorideHCID 70091tert-Butyl carbazateHCID 10929713-(Dimethyl-1,2-oxazol-4-yl)propanoic acid

생성물 2

HCID 222AmmoniaHCID 59347450tert-Butyl 2-[3-(3,5-dimethylisoxazol-4-yl)propanoyl]hydrazinecarboxylate

시약·촉매·용매 2

HCID 6228Dimethylformamide
촉매
HCID 6344Dichloromethane용매3회

실험 절차

Oxalyl chloride (5.16 mL, 59.2 mmol) was added to a solution of β-(3,5-dimethyl-4-isoxazolyl)propionic acid (J. Org. Chem. 59(10); 1994; 2882) (2.5 g, 14.8 mmol) in dichloromethane (50 mL) and N,N-dimethylformamide (1 drop), and the solution was stirred at room temperature for 30 minutes. The mixture was concentrated under reduced pressure and the residue was azeotroped with dichloromethane (5×) to provide a brown liquid. This was dissolved in dichloromethane (25 mL), and tert-butyl carbazate (2.93 g, 22.2 mmol) was added portionwise. The mixture was diluted with further dichloromethane (23 mL) and the reaction was stirred for 18 hours at room temperature. The mixture was concentrated under reduced pressure, the residue was suspended in dichloromethane, the resulting precipitate was filtered off and the filtrate was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol:0.88 ammonia (95:5:0.5 to 90:10:1) to provide the title compound as an oil, 3.08 g.

후처리

  1. concentrationThe mixture was concentrated under reduced pressure
  2. customthe residue was azeotroped with dichloromethane (5×)
  3. customto provide a brown liquid
  4. stirringthe reaction was stirred for 18 hours at room temperature
  5. concentrationThe mixture was concentrated under reduced pressure
  6. filtrationthe resulting precipitate was filtered off
  7. customthe filtrate was evaporated under reduced pressure
  8. customThe residue was purified by column chromatography on silica gel using an elution gradient of dichloromethane

출처 및 근거

ORD 기록
ord-117c4b75dcf64cb89e8a6717ed6ced75
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08093400B2

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