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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80730생성일: 2026년 10월 23일

Tert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylate → tert-Butyl 5-[3-(2-aminopyrid-4-yl)-2-(4-chlorophenyl)imidazo[1,2-b]pyridazin-6-yl]hexahydropyrrolo[3,4-c]pyrrole-2-carboxylate

https://huagongshe.com/ko/reaction/80730

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
반응물4-[6-Chloro-2-(4-chlorophenyl)imidazo[1,2-b]pyridazin-3-yl]pyrid-2-ylamineHCID 59406950—
용매1-PentanolHCID 6276—
생성물tert-Butyl 5-[3-(2-aminopyrid-4-yl)-2-(4-chlorophenyl)imidazo[1,2-b]pyridazin-6-yl]hexahydropyrrolo[3,4-c]pyrrole-2-carboxylateHCID 5940695371.6%

반응 조건

온도135 °C

반응 단계

A mixture of 0.15 g (0.42 mmol) of 4-[6-chloro-2-(4-chlorophenyl)imidazo[1,2-b]pyridazin-3-yl]pyrid-2-ylamine and 0.36 g (1.7 mmol) of tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2-carboxylate in 7 mL of pentanol is stirred at 135° C. for 20 hours. The solvent is then evaporated off under reduced pressure and the oily residue is chromatographed on a column of silica gel, eluting with a stepwise gradient of methanol and aqueous ammonia in dichloromethane (0:0:100 to 2:1:98). 0.16 g of product is isolated after trituration in diisopropyl ether, filtering off and drying under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846676B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2a30010c88fe4cd29478672b484c4d43
출처 메모uspto-grants-2014_09