反応 #1867

反応方程式

trans- 7-chloro-5-(2-chlorophenyl)-1-isobutyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid

pivaloyloxymethyl chloride

N,N-diisobutyl ethylamine

water

→

trans-7-chloro-5-(2-chlorophenyl)-1-isobutyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid pivaloyloxymethyl ester

溶媒

N,N-dimethylformamide

ethyl acetate

反応条件

後処理

1. 1
   抽出followed by extraction
2. 2
   洗浄The ethyl acetate layer was washed with an aqueous solution of potassium hydrogensulfate
3. 3
   乾燥an aqueous solution of sodium hydrogencarbonate and water, successively, which was dried over anhydrous magnesium sulfate
4. 4
   workup.DISTILLATIONThe solvent was then distilled off under reduced pressure
5. 5
   その他The residue was purified by means of a silica gel column chromatography (hexane:ethyl acetate=10:1 to 5:1)

実験手順

In N,N-dimethylformamide (10 ml) was dissolved trans- 7-chloro-5-(2-chlorophenyl)-1-isobutyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid (0.5 g) obtained in Example 2. To the solution were added pivaloyloxymethyl chloride (0.43 ml), N,N-diisobutyl ethylamine (0.52 ml) and KI (0.2 g). The mixture was stirred at room temperature overnight. To the reaction mixture were added water (100 ml) and ethyl acetate (100 ml), followed by extraction. The ethyl acetate layer was washed with an aqueous solution of potassium hydrogensulfate, an aqueous solution of sodium hydrogencarbonate and water, successively, which was dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (hexane:ethyl acetate=10:1 to 5:1) to afford trans-7-chloro-5-(2-chlorophenyl)-1-isobutyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid pivaloyloxymethyl ester (0.55 g).

出典