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

HRID 965787
ノート
印刷プレビュー

反応式

HRID 965787 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒

反応条件

温度
70 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-85098460e20c44b8ace93eb81d576e84
出典データセット
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06951867B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート