Acetic Acid → N-(4-dipropylaminobutyl)-4-{[(1H-imidazol-2-ylmethyl)-(2R)-pyrrolidin-2-ylmethylamino]-methyl}-benzamide

HRID 348614

反応式

HRID 348614 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH2:6][NH:7][CH2:8][C:9]1[CH:28]=[CH:27][CH:26]=[CH:25][C:10]=1C(NCCCCN(CCC)CCC)=O.C([O:34][CH3:35])(OC)OC.C([N:43]1[CH2:49][CH2:48][CH2:47][C@@H:44]1[CH:45]=O)(OC(C)(C)C)=O.[C:50]([BH3-])#[N:51].[Na+].[C:54](O)(=O)[CH3:55]>CO>[CH2:26]([N:51]([CH2:50][CH2:54][CH3:55])[CH2:25][CH2:10][CH2:9][CH2:8][NH:7][C:35](=[O:34])[C:26]1[CH:25]=[CH:10][C:9]([CH2:8][N:7]([CH2:6][C:2]2[NH:1][CH:5]=[CH:4][N:3]=2)[CH2:45][C@H:44]2[CH2:47][CH2:48][CH2:49][NH:43]2)=[CH:28][CH:27]=1)[CH2:27][CH3:28]

参加物

7

反応物 5

HCID 176Acetic AcidHCID 9005Trimethyl orthoformateHCID 5003444Sodium cyanoborohydrideHCID 7009153N-(tert-Butoxycarbonyl)-D-prolinalHCID 86599830HCID 86599830、化合物

生成物 1

HCID 58801900N-(4-dipropylaminobutyl)-4-{[(1H-imidazol-2-ylmethyl)-(2R)-pyrrolidin-2-ylmethylamino]-methyl}-benzamide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

The compound (53.8 mg) obtained in Example 1-4 was dissolved in methanol (0.8 ml). Then, the solution was added with trimethyl orthoformate (50 μl), acetic acid (50 μl), N-Boc-D-prolinal (manufactured by Aldrich Corporation) (25.7 mg) and stirred at room temperature for 10 minutes. Subsequently, sodium cyanoborohydride (24.4 mg) was added, followed by stirring overnight at room temperature. The solvent was distilled off under reduced pressure and the residue was then dissolved in chloroform, followed by washing with 1 mol/l sodium hydroxide and saturated saline solution and drying with anhydrous sodium sulfate. After filtration, the solvent was distilled off under reduced pressure and the residue was then purified through silica gel column chromatography (chloroform/methanol). Then, the purified product was dissolved in methanol (500 μl) and added with a 4 mol/l hydrogen chloride/dioxane solution (500 μl), followed by stirring at room temperature for 2 hours. After completion of the reaction, the solvent was distilled off under reduced pressure and the residue was then purified through silica gel column chromatography (chloroform/methanol), thereby obtaining hydrochloride (33.9 mg) of the subject compound as a white solid.

後処理

  1. stirringby stirring overnight at room temperature
  2. distillationThe solvent was distilled off under reduced pressure
  3. dissolutionthe residue was then dissolved in chloroform
  4. washby washing with 1 mol/l sodium hydroxide and saturated saline solution
  5. dry with materialdrying with anhydrous sodium sulfate
  6. filtrationAfter filtration
  7. distillationthe solvent was distilled off under reduced pressure
  8. customthe residue was then purified through silica gel column chromatography (chloroform/methanol)
  9. dissolutionThen, the purified product was dissolved in methanol (500 μl)
  10. additionadded with a 4 mol/l hydrogen chloride/dioxane solution (500 μl)
  11. stirringby stirring at room temperature for 2 hours
  12. customAfter completion of the reaction
  13. distillationthe solvent was distilled off under reduced pressure
  14. customthe residue was then purified through silica gel column chromatography (chloroform/methanol)

出典と根拠

ORDレコード
ord-0cd58ac9eb2e46c4880960324804f548
出典データセット
uspto-grants-2007_02
特許番号
US07176227B2

関連ノート

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