Dimethylformamide → Methyl 6-{propyl[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}nicotinate

HRID 1025438ノート

反応式

HRID 1025438 の反応式
[CH3:1][Si:2]([CH3:29])([CH3:28])[CH2:3][CH2:4][O:5][C:6]([C:8]1[CH:9]=[C:10]([S:14]([NH:17][C:18]2[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][N:19]=2)(=[O:16])=[O:15])[CH:11]=[CH:12][CH:13]=1)=[O:7].CN(C=O)C.I[CH2:36][CH2:37][CH3:38].C(=O)([O-])[O-].[K+].[K+]>O>[CH2:36]([N:17]([S:14]([C:10]1[CH:11]=[CH:12][CH:13]=[C:8]([C:6]([O:5][CH2:4][CH2:3][Si:2]([CH3:28])([CH3:1])[CH3:29])=[O:7])[CH:9]=1)(=[O:15])=[O:16])[C:18]1[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][N:19]=1)[CH2:37][CH3:38]

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 336431-IodopropaneHCID 71238735Methyl 6-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}nicotinate

生成物 1

HCID 71238187Methyl 6-{propyl[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}nicotinate

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
80 °C

実験手順

To a mixture of 500 mg of methyl 6-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}nicotinate and 10 mL of DMF were added 0.300 mL of 1-iodopropane and 400 mg of potassium carbonate, followed by stirring at 80° C. for 5 hours. The reaction mixture was left to stand to cool and then water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, and then dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and then the residue was purified by silica gel column chromatography (chloroform-ethyl acetate) to obtain 200 mg of a methyl 6-{propyl[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}nicotinate as a colorless oily substance. ESI+: 479

後処理

  1. waitThe reaction mixture was left
  2. temperatureto cool
  3. extractionfollowed by extraction with ethyl acetate
  4. washThe organic layer was washed with saturated brine
  5. dry with materialdried over magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (chloroform-ethyl acetate)

出典と根拠

ORDレコード
ord-29925f5bf4bf4ea8add63bf521778469
出典データセット
uspto-grants-2014_05
特許番号
US08729068B2

反応ノート

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