Benzyl Chloride → HCID 485902、化合物
反応式
[Cl:1][C:2]1[C:20]([Cl:21])=[CH:19][C:5]2[N:6]([C@@H:10]3[O:16][C@H:15]([CH2:17][OH:18])[C@@H:13]([OH:14])[C@H:11]3[OH:12])[C:7](=[S:9])[NH:8][C:4]=2[CH:3]=1.[OH-].[NH4+].[CH2:24](Cl)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.C(Cl)Cl.CO>O>[CH2:24]([S:9][C:7]1[N:6]([C@@H:10]2[O:16][C@H:15]([CH2:17][OH:18])[C@@H:13]([OH:14])[C@H:11]2[OH:12])[C:5]2[CH:19]=[C:20]([Cl:21])[C:2]([Cl:1])=[CH:3][C:4]=2[N:8]=1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1参加物
実験手順
Compound 53 (0.5 g) was dissolved in cold water (10 ml) containing concentrated ammonium hydroxide (2.5 ml). Benzyl chloride (0.5 ml) was added to this solution with stirring and the stirring continued at room temperature for 5 hours. The white solid (0.41 g) which had separated from solution was collected by filtration, washed with cold water. The solid was extracted with ethyl acetate (100 ml) and the ethyl acetate phase was dried over anhydrous Na2SO4 and then evaporated by aspirator to give a syrup. The syrup was subjected to a flash column of silica gel with CH2Cl2 -MeOH (15:1) as eluant. Fractions were collected (25 ml each) and fractions containing the desired compound were combined and evaporated to afford 54 which was crystallized from CH2Cl2 -MeOH (15:1), mp. 149° C., Yield 0.223 g (35.5%).
後処理
- customThe white solid (0.41 g) which had separated from solution
- filtrationwas collected by filtration
- washwashed with cold water
- extractionThe solid was extracted with ethyl acetate (100 ml)
- dry with materialthe ethyl acetate phase was dried over anhydrous Na2SO4
- customevaporated by aspirator
- customto give a syrup
- customFractions were collected (25 ml each) and fractions
- additioncontaining the desired compound
- customevaporated
出典と根拠
- ORDレコード
- ord-a58ead1c61e84223ba67e0cbd81391ce
- 出典データセット
- uspto-grants-1994_11
- 特許番号
- US05360795
反応ノート
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