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HRID 1087089作成日:2026年10月27日

Ammonia → cis-(+-)-N-(2-(2,6-Dimethyl-1-piperidinyl)ethyl)-2-oxo-3-hydroxy-1-pyrrolidineacetamide

https://huagongshe.com/reaction/1087089

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物(R/S)-cis-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetamideHCID 53715870—
溶媒MethanolHCID 887—
生成物cis-(+-)-N-(2-(2,6-Dimethyl-1-piperidinyl)ethyl)-2-oxo-3-hydroxy-1-pyrrolidineacetamideHCID 3069833—

反応手順

0.3 g of (R/S)-cis-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-acetoxy-2-oxo-1-pyrrolidinyl)acetamide is stirred at room temperature for 2 hours in 30 ml of a saturated solution of ammonia in methanol. After evaporation of the methanol, the residue is treated three times with toluene and in each case again evaporated. After trituration in diethyl ether, there is obtained (R/S)-cis-N-[2(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetamide of melting point 129°-130°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05034402
出典データセットuspto-grants-1991_07
ORD IDord-f6a723b8bdd24b6c8d501c627b23f5d2
出典メモuspto-grants-1991_07