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HRID 1873549생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 68626191—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-Cyano-5-ethyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 6862547748.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304411B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-9fdf72cc277e4070a52202139790eb2c
출처 메모uspto-grants-2012_11