Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1961603생성일: 2026년 10월 26일
Iodocyclopentane → 5-Cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide
https://huagongshe.com/reaction/1961603
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodocyclopentane | HCID 73784 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | 5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide | HCID 68626191 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-Cyano-5-cyclopentyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide | HCID 68625827 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08415349B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-c4db9e08703f41afbb514a26c29d97cc |
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| 출처 메모 | uspto-grants-2013_04 |
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