Trimethyl orthoformate → N'-({1-[4-(dipropylamino)butyl]-4-piperidinyl}methyl)-N,N-bis(1H-imidazol-2-ylmethyl)urea

HRID 1897633ノート

反応式

HRID 1897633 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH2:6][N:7]([CH2:18][C:19]1[NH:20][CH:21]=[CH:22][N:23]=1)[C:8]([NH:10][CH2:11][CH:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1)=[O:9].[CH2:24]([N:27]([CH2:33][CH2:34][CH3:35])[CH2:28][CH2:29][CH2:30][CH:31]=O)[CH2:25][CH3:26].C(OC)(OC)OC.[BH4-].[Na+]>CO>[CH2:33]([N:27]([CH2:24][CH2:25][CH3:26])[CH2:28][CH2:29][CH2:30][CH2:31][N:15]1[CH2:16][CH2:17][CH:12]([CH2:11][NH:10][C:8](=[O:9])[N:7]([CH2:18][C:19]2[NH:20][CH:21]=[CH:22][N:23]=2)[CH2:6][C:2]2[NH:1][CH:5]=[CH:4][N:3]=2)[CH2:13][CH2:14]1)[CH2:34][CH3:35]

参加物

6

反応物 4

HCID 9005Trimethyl orthoformateHCID 4311764Sodium borohydrideHCID 226111444-(Dipropylamino)butanalHCID 67502645N,N-bis(1H-imidazol-2-ylmethyl)-N'-(piperidin-4-ylmethyl)urea

生成物 1

HCID 57764673N'-({1-[4-(dipropylamino)butyl]-4-piperidinyl}methyl)-N,N-bis(1H-imidazol-2-ylmethyl)urea収率 34.4%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Under an argon atmosphere, to a methanol (2.3 mL) solution of the compound (73 mg) obtained in Example 10, 4-(dipropylamino)butanal (39 mg) and trimethyl orthoformate (49 mg) were added at 0° C. The reaction solution was stirred at room temperature for 2 hours. To the reaction solution, sodium borohydride (17 mg) was added at 0° C., followed by stirring for one hour. The reaction solution was concentrated under reduced pressure, and then an aqueous 5N sodium hydroxide solution (10 mL) was added to the residue. The aqueous layer was extracted twice with chloroform (30 mL). The combined organic layer was dried over anhydrous magnesium sulfate. After removing the anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by silica gel chromatography (dichrolomethane:methanol:28% aqueous ammonia=10:1:0→80:10:1) to obtain the title compound (37 mg) having the following physical properties.

後処理

  1. stirringby stirring for one hour
  2. concentrationThe reaction solution was concentrated under reduced pressure
  3. additionan aqueous 5N sodium hydroxide solution (10 mL) was added to the residue
  4. extractionThe aqueous layer was extracted twice with chloroform (30 mL)
  5. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  6. customAfter removing the anhydrous sodium sulfate
  7. filtrationby filtration
  8. concentrationthe filtrate was concentrated
  9. customThe residue was purified by silica gel chromatography (dichrolomethane:methanol:28% aqueous ammonia=10:1:0→80:10:1)

出典と根拠

ORDレコード
ord-64f1e364e2d548c6847b601146765231
出典データセット
uspto-grants-2013_08
特許番号
US08519124B2

反応ノート

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