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3-Dimethylsulfamoyl-5-trifluoromethyl-benzoic acid → Methyl 2-(3-(N,N-dimethylsulfamoyl)-N-(2-methoxy-3,4'-bipyridin-3'-yl)-5-(trifluoromethyl)benzamido)acetate

HRID 878202
ノート
印刷プレビュー

反応式

HRID 878202 の反応式
[CH3:1][O:2][C:3](=[O:20])[CH2:4][NH:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][C:11]=1[C:12]1[C:13]([O:18][CH3:19])=[N:14][CH:15]=[CH:16][CH:17]=1.[CH3:21][N:22]([CH3:39])[S:23]([C:26]1[CH:27]=[C:28]([CH:32]=[C:33]([C:35]([F:38])([F:37])[F:36])[CH:34]=1)[C:29](O)=[O:30])(=[O:25])=[O:24]>>[CH3:21][N:22]([CH3:39])[S:23]([C:26]1[CH:27]=[C:28]([CH:32]=[C:33]([C:35]([F:37])([F:36])[F:38])[CH:34]=1)[C:29]([N:5]([CH2:4][C:3]([O:2][CH3:1])=[O:20])[C:6]1[CH:7]=[N:8][CH:9]=[CH:10][C:11]=1[C:12]1[C:13]([O:18][CH3:19])=[N:14][CH:15]=[CH:16][CH:17]=1)=[O:30])(=[O:24])=[O:25]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 179640083-Dimethylsulfamoyl-5-trifluoromethyl-benzoic acidHCID 70663573Methyl 2-(4-(2-methoxypyridin-3-yl)pyridin-3-ylamino)acetate

生成物 1

HCID 70663565Methyl 2-(3-(N,N-dimethylsulfamoyl)-N-(2-methoxy-3,4'-bipyridin-3'-yl)-5-(trifluoromethyl)benzamido)acetate

実験手順

The title compound was prepared in analogy to example 90, from (2-methoxy-[3,4′]bipyridinyl-3′-ylamino)-acetic acid methyl ester and 3-dimethylsulfamoyl-5-trifluoromethyl-benzoic acid (Buttpark Ltd.) after a reaction time of 72 hours. The compound was purified by silica gel chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:EtOAc (100:0 to 20:80). The product-containing fractions were pooled and evaporated and the residue poured on 30 mL 1M aqueous HCl and 30 mL EtOAc. The layers were separated and the aqueous layer was extracted a second time with 30 mL EtOAc. The organic layers were washed twice with 30 mL 1M aqueous HCl followed by 30 mL brine, dried over MgSO4, filtered and concentrated under vacuum. Light yellow solid (30%). MS (ESI): m/z=553.135 [M+H]+.

後処理

  1. customThe compound was purified by silica gel chromatography
  2. washeluting with a gradient of n-heptane:EtOAc (100:0 to 20:80)
  3. customevaporated
  4. additionthe residue poured on 30 mL 1M aqueous HCl and 30 mL EtOAc
  5. customThe layers were separated
  6. extractionthe aqueous layer was extracted a second time with 30 mL EtOAc
  7. washThe organic layers were washed twice with 30 mL 1M aqueous HCl
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-2ba0e040800641aebc8c6c6c56a568dd
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987307B2

反応ノート

読み込み中…

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