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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 402683생성일: 2026년 10월 26일

Chloroacetyl chloride → propan-2-yl 2-(cyclohexylamino)-4-oxo-5-(1H-pyrrolo[2,3-b]pyridin-3-ylmethylidene)furan-3-carboxylate

https://huagongshe.com/reaction/402683

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetyl chlorideHCID 6577—
반응물CyclohexylamineHCID 7965—
반응물PiperidineHCID 8082—
반응물Diisopropyl malonateHCID 83223—
반응물1H-Pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 5372812—
반응물Isopropyl 2-isopropoxy-4-oxo-4,5-dihydrofuran-3-carboxylateHCID 51050080—
용매IsopropanolHCID 3776—
생성물propan-2-yl 2-(cyclohexylamino)-4-oxo-5-(1H-pyrrolo[2,3-b]pyridin-3-ylmethylidene)furan-3-carboxylateHCID 1784594084.5%

반응 단계

A solution of isopropyl 2-isopropoxy-4-oxo-4,5-dihydrofuran-3-carboxylate (0.10 g, 0.44 mmol) which similarly prepared according to the procedure described in the Example 74, Third step using diisopropyl malonate and chloroacetyl chloride, and cyclohexylamine (0.055 mL, 0.48 mmol) in 2-propanol (2.0 mL) was stirred at ambient temperature for 14 h. To this reaction mixture, 7-azaindole-3-carboxaldehyde (0.065 g, 0.44 mmol) and piperidine (0.0044 mL, 0.044 mmol) were added then the mixture was refluxed for further 8 days. Cooled to ambient temperature, the reaction mixture was purified by preparative HPLC to afford the titled compound as solid (0.0079 g, y. 4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08742113B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-486f09d95e5c4967901e330da4bade40
출처 메모uspto-grants-2014_06