Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1734103생성일: 2026년 10월 26일
Dicyclohexylcarbodiimide → 6-Amidino-2-naphthyl 5-(3-t-butoxycarbonylpropionylaminomethyl)furan-2-carboxylate hydrochloride
https://huagongshe.com/reaction/1734103
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | Butanedioic acid,1-(1,1-dimethylethyl) ester | HCID 22317022 | — |
| 반응물 | 6-Amidino-2-naphthyl 5-aminomethylfuran-2-carboxylate dihydrochloride | HCID 22398815 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 6-Amidino-2-naphthyl 5-(3-t-butoxycarbonylpropionylaminomethyl)furan-2-carboxylate hydrochloride | HCID 22398804 | 68% |
반응 단계
To 11.4 g of mono-t-butyl succinate, 23.5 g of 6-amidino-2-naphthyl 5-aminomethylfuran-2-carboxylate dihydrochloride and 0.66 g of DMAP was added 115 ml of pyridine, and the mixture was stirred with ice-cooling. After 10 minutes, 25.6 g of DCC was added and the mixture was stirred for 3 hours while cooling with ice and for 16 hours at room temperature. The precipitated crystals were filtered off, and the filtrate was added in small portions into 2 l of ether and stirred at room temperature for 3 l hours. After removing the supernatant by decantation, 1 l of acetone was added to the residue and stirred for 1 hour. The precipitate was collected by filtration, then dissolved in 60 ml of methanol and 3 g of active carbon was added to the solution. The mixture was stirred for 30 minutes while cooling with ice, then the insolubles were filtered off and the filtrate was added into 1.5 l of acetone. The mixture was stirred for 5 hours while cooling with ice, and the precipitated crystals were collected by filtration to obtain 21 g of the intended product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05532267 |
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| 출처 데이터셋 | uspto-grants-1996_07 |
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| ORD ID | ord-22d060cde1e242b9bb63d61a2702ae1f |
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| 출처 메모 | uspto-grants-1996_07 |
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