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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1873541생성일: 2026년 10월 26일

Iodocyclopentane → 5-Cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

https://huagongshe.com/reaction/1873541

반응식

참여 물질

역할이름HCID투입량
반응물IodocyclopentaneHCID 73784—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 68626191—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-Cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 6862582742%

반응 단계

5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 12a was dissolved in 30 mL of N,N-dimethylformamide followed by addition of iodo-cyclopentane (5.4 g, 27.5 mmol) and lithium hexamethyldisilazide (27.5 mL, 27.5 mmol) under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was diluted with 10 mL of water and concentrated to remove N,N-dimethylformamide and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 5-cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 16a (2.6 g, yield 42%) as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304411B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-3cc2244656264d7a8c24fac657b8f5cf
출처 메모uspto-grants-2012_11