反応式
[OH:1][CH2:2][CH:3]1[CH2:7][CH2:6][NH:5][CH2:4]1.[CH2:8]([O:15][C:16]([NH:18][C:19](=[NH:22])OC)=[O:17])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>C1(C)C=CC=CC=1>[CH2:8]([O:15][C:16]([NH:18][C:19]([N:5]1[CH2:6][CH2:7][CH:3]([CH2:2][OH:1])[CH2:4]1)=[NH:22])=[O:17])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1参加物
反応条件
- 温度
- 60 °C
実験手順
1.01 g (0.01 mole) (3RS)-3-hydroxymethyl pyrrolidine and 2.29 g (0.011 mole) N-benzyloxycarbonyl-O-methylisourea was dissolved (the amine not very soluble) in toluene and heated to 60° C. for three hours followed by stirring at room temperature over night. The mixture was evaporated and the 1H-NMR showed that the reaction was not completed. The mixture was therefore dissolved in 15 ml acetonitrile and heated to 60° C. for three hours followed by stirring at room temperature over night. The solvent was evaporated and the mixture was dissolved in CH2Cl2, washed once with water, dried (Na2SO4), filtered and evaporated. The crude product was purified by flash chromatography using CH2Cl2 /MeOH 95/5 as eluent to yield 0.70 g (25%) of the product.
後処理
- customThe mixture was evaporated
- dissolutionThe mixture was therefore dissolved in 15 ml acetonitrile
- temperatureheated to 60° C. for three hours
- stirringby stirring at room temperature over night
- customThe solvent was evaporated
- dissolutionthe mixture was dissolved in CH2Cl2
- washwashed once with water
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated
- customThe crude product was purified by flash chromatography
出典と根拠
- ORDレコード
- ord-5b550e99bd8a4e83aecd2baa957c8fb1
- 出典データセット
- uspto-grants-1999_01
- 特許番号
- US05856307
関連ノート
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