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Methylamine → N-methyl-1-(4-{5-[3-(trifluoromethyl)-4-(2,2,2-trifluoro-1-methylethoxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-3-yl)methanamine

HRID 552855
ノート
印刷プレビュー

反応式

HRID 552855 の反応式
[F:1][C:2]([F:33])([F:32])[C:3]1[CH:4]=[C:5]([C:16]2[O:20][N:19]=[C:18]([C:21]3[CH:29]=[CH:28][CH:27]=[C:26]4[C:22]=3[C:23]([CH:30]=O)=[CH:24][NH:25]4)[N:17]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH:10]([CH3:15])[C:11]([F:14])([F:13])[F:12].[CH3:34][NH2:35]>CO>[CH3:34][NH:35][CH2:30][C:23]1[C:22]2[C:26](=[CH:27][CH:28]=[CH:29][C:21]=2[C:18]2[N:17]=[C:16]([C:5]3[CH:6]=[CH:7][C:8]([O:9][CH:10]([CH3:15])[C:11]([F:14])([F:12])[F:13])=[C:3]([C:2]([F:33])([F:32])[F:1])[CH:4]=3)[O:20][N:19]=2)[NH:25][CH:24]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6329MethylamineHCID 592144034-{5-[3-(trifluoromethyl)-4-(2,2,2-trifluoro-1-methylethoxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indole-3-carboaldehyde

生成物 1

HCID 59214308N-methyl-1-(4-{5-[3-(trifluoromethyl)-4-(2,2,2-trifluoro-1-methylethoxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-3-yl)methanamine収率 56.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a solution of 4-{5-[3-(trifluoromethyl)-4-(2,2,2-trifluoro-1-methylethoxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indole-3-carboaldehyde (150.0 mg) in CH3OH (1.5 ml) was added a 40% CH3OH solution of CH3NH2 (74.5 mg) at 0° C. After warming to room temperature, the solution was stirred at room temperature for 3 hours. After confirming the production of an iminium salt, the organic solvent was evaporated under reduced pressure. The residue was dissolved in EtOH (1.5 ml). To this was added NaBH4 (12.09 mg) at 0° C. After warming to room temperature, the solution was stirred at room temperature for 15 hours. To the reaction solution was added water (30 ml), followed by extraction three times with EtOAc (20 ml). The organic layer was combined, washed with saturated brine, dried over anhydrous MgSO4, and then filtered, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (automatic purifier, chloroform:CH3OH=100:0 to 90:10) to obtain N-methyl-1-(4-{5-[3-(trifluoromethyl)-4-(2,2,2-trifluoro-1-methylethoxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-3-yl)methanamine (87.4 mg) as a white solid.

後処理

  1. customthe organic solvent was evaporated under reduced pressure
  2. dissolutionThe residue was dissolved in EtOH (1.5 ml)
  3. additionTo this was added NaBH4 (12.09 mg) at 0° C
  4. temperatureAfter warming to room temperature
  5. stirringthe solution was stirred at room temperature for 15 hours
  6. additionTo the reaction solution was added water (30 ml)
  7. extractionfollowed by extraction three times with EtOAc (20 ml)
  8. washwashed with saturated brine
  9. dry with materialdried over anhydrous MgSO4
  10. filtrationfiltered
  11. concentrationthe filtrate was concentrated
  12. customThe residue was purified by silica gel column chromatography (automatic purifier, chloroform:CH3OH=100:0 to 90:10)

出典と根拠

ORDレコード
ord-8f1a85eebfe8418087754c10236b65a4
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07951825B2

反応ノート

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