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HRID 1743260作成日:2026年10月27日

Ammonium Chloride → Tert-butyl (3r,5r,6s)-2-oxo-5,6-diphenyl-3-[1-(2-trimethylsilanyl-ethoxycarbonyl)piperidin-4-yl]morpholine-4-carboxylate

https://huagongshe.com/reaction/1743260

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物15-Crown-5HCID 36336—
反応物tert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylateHCID 981230—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物2-Trimethylsilanylethyl 4-iodopiperidine-1-carboxylateHCID 22238408—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl (3r,5r,6s)-2-oxo-5,6-diphenyl-3-[1-(2-trimethylsilanyl-ethoxycarbonyl)piperidin-4-yl]morpholine-4-carboxylateHCID 90791180—

反応条件

温度-78 °C

反応手順

4 g of tert-butyl (5S,6R)-2-oxo-5,6-diphenylmorpholine-4-carboxylate were dissolved in 50 ml of THF. 9 ml of 15-crown-5 were added, and the mixture was cooled to −78° C. Then 6.8 ml of a 2 M solution of NaHMDS in THF were added dropwise. The mixture was stirred for 10 min and then 8 g of 2-trimethylsilanylethyl 4-iodopiperidine-1-carboxylate were added dropwise. The mixture was allowed to warm to 0° C. over the course of 6 h, and then the reaction was stopped by adding 200 ml of saturated ammonium chloride solution. The aqueous phase was extracted 3 times with 150 ml of ethyl acetate each time, and the combined organic phases were dried with MgSO4. The solvents were removed in vacuo, and the residue was chromatographed on silica gel.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07008957B2
出典データセットuspto-grants-2006_03
ORD IDord-3e41b89821224680bb8e0715a9e0af01
出典メモuspto-grants-2006_03