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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

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Butanedioic acid,1-(1,1-dimethylethyl) esterHCID 22317022—
반응물6-Amidino-2-naphthyl 5-aminomethylfuran-2-carboxylate dihydrochlorideHCID 22398815—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
생성물6-Amidino-2-naphthyl 5-(3-t-butoxycarbonylpropionylaminomethyl)furan-2-carboxylate hydrochlorideHCID 2239880468%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05532267
출처 데이터셋uspto-grants-1996_07
ORD IDord-22d060cde1e242b9bb63d61a2702ae1f
출처 메모uspto-grants-1996_07