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Ammonia → Ethyl 2-amino-6-[(2,2-dimethylpropanoyl)amino]nicotinate

HRID 965787
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HRID 965787 반응식
[CH3:1][C:2]([CH3:19])([CH3:18])[C:3]([NH:5][C:6]1[CH:16]=[CH:15][C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[C:8](F)[N:7]=1)=[O:4].[NH3:20].O>CC(O)C>[NH2:20][C:8]1[N:7]=[C:6]([NH:5][C:3](=[O:4])[C:2]([CH3:19])([CH3:18])[CH3:1])[CH:16]=[CH:15][C:9]=1[C:10]([O:12][CH2:13][CH3:14])=[O:11]
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참가 물질

5

반응물 3

HCID 222AmmoniaHCID 962WaterHCID 15893123Ethyl 2-fluoro-6-pivaloylaminopyridine-3-carboxylate

생성물 1

HCID 12088088Ethyl 2-amino-6-[(2,2-dimethylpropanoyl)amino]nicotinate수율 55%

시약·촉매·용매 1

HCID 3776Isopropanol용매

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온도
70 °C

실험 절차

To a stirred solution of ethyl 6-[(2,2-dimethylpropanoyl)amino]-2-fluoronicotinate (M. C. Coldwell et al., Bioorg. Med. Chem. Lett., 1995, 39, 5, 1.5 g, 5.59 mmol) in 2-propanol (16 mL) was added 25% aqueous ammonia (4 mL) and the mixture was heated in a sealed tube at 70° C. for 4.5 h. After cooling to room temperature, water was added and the mixture was extracted with ethyl acetate. The separated organic layer was concentrated in vacuo and the residue was chromatographed on a column of silica gel eluting with ethyl acetate/pentane (1:6 to 1:2) to give 810 mg (55%) of the title compound as a white solid.

후처리

  1. temperatureAfter cooling to room temperature
  2. extractionthe mixture was extracted with ethyl acetate
  3. concentrationThe separated organic layer was concentrated in vacuo
  4. customthe residue was chromatographed on a column of silica gel eluting with ethyl acetate/pentane (1:6 to 1:2)

출처 및 근거

ORD 기록
ord-85098460e20c44b8ace93eb81d576e84
출처 데이터셋
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06951867B2

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