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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220358생성일: 2026년 10월 24일

Potassium Carbonate → HCID 58180582, 화합물

https://huagongshe.com/ko/reaction/220358

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Benzoyl isothiocyanateHCID 68284—
반응물2-Bromo-1-(2-pyridinyl)-1-ethanone hydrobromideHCID 2776231—
반응물4-amino-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamideHCID 58180503—
용매AcetoneHCID 180—
생성물HCID 58180582HCID 5818058210%

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온도60 °C

반응 단계

A solution of 4-amino-N,N-dicyclopropyl-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (example 1J, 70 mg, 0.21 mmol) and benzoyl isothiocyanate (36 μl, 0.27 mmol) in acetone (1 ml) was stirred at room temperature for 1.5 h. The solvent was removed in vacuo, the residue was taken up in EtOH (1.5 ml), and K2CO3 (40 mg, 0.290 mmol) was added. The reaction was heated at 60° C. for 3 h. Upon cooling to room temperature, 2-bromo-1-(pyridin-2-yl)ethanone, hydrobromide (139.4 mg, 0.50 mmol) was added and the reaction heated at 80° C. for 24 h. The reaction mixture was cooled to room temperature and concentrated. The residue was purified by silica gel chromatography (0-7% MeOH/dichloromethane). Re-purification by preparative HPLC provided 10.2 mg (10% yield) of N,N-dicyclopropyl-6-ethyl-1-methyl-4-(4-(pyridin-2-yl)thiazol-2-ylamino)-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202881B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-784294f13ca14d49a5ece0fc2b4d2b57
출처 메모uspto-grants-2012_06