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HRID 1873549作成日:2026年10月24日

Iodoethane → 5-Cyano-5-ethyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

https://huagongshe.com/ja/reaction/1873549

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 68626191—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-Cyano-5-ethyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 6862547748.1%

反応手順

5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 12a (3.0 g, 14.5 mmol) was dissolved in 60 mL of tetrahydrofuran with stirring followed by addition of ethyl iodide (4.52 g, 29 mmol) and lithium hexamethyldisilazide (29 mL, 29 mmol) under nitrogen atmosphere. The reaction mixture was reacted at room temperature for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was diluted with 20 mL of water and extracted with ethyl acetate (200 mL×3). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtain an oil. TLC showed that there are two adjacent spots, and then the oil was purified by silica gel column chromatography to obtain the title compound 5-cyano-5-ethyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 19a (1.64 g) as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304411B2
出典データセットuspto-grants-2012_11
ORD IDord-9fdf72cc277e4070a52202139790eb2c
出典メモuspto-grants-2012_11