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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 649539생성일: 2026년 10월 24일

Iodine → HCID 20141777, 화합물

https://huagongshe.com/ko/reaction/649539

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Potassium CarbonateHCID 11430—
반응물3-Bromoquinolin-2-olHCID 268338—
반응물6-Bromo-8-methylquinolin-2(1H)-oneHCID 13836183—
반응물HCID 178467223HCID 178467223—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물HCID 20141777HCID 20141777—

반응 단계

A mixture of 6-bromo-8-methyl-2-(1H)-quinolone (2.38 g), (see Preparation 67 of European patent application publication No. 0148623), 4-acetyl-2-methylimidazole (2.48 g), finely divided copper-bronze (0.64 g), potassium carbonate (1.38 g), and a few crystals of iodine was stirred and heated in N-methyl-2-pyrrolidone (8 cm3) at 190° C. for 24 hours under nitrogen. The cooled mixture was then poured into methanol:dichloromethane (100 cm3, 1:10 by volume), stirred and filtered. The filtrate was poured into aqueous ammonia (20 cm3, S.G. 0.880) and the mixture was filtered through "Solkafloc" (Trademark for a cellulose-based filtering aid). The filtrate was separated and the aqueous phase was re-extracted with methanol:dichloromethane (3×100 cm3), 1:10 by volume). The combined and dried (MgSO4) organic extracts were evaporated in vacuo to give a residue which was chromatographed on silica (Merck "MK 60.9385" [Trademark]). Elution with methanol:dichloromethane, 1:33 by volume, followed by combination and evaporation of the appropriate fractions, gave unreacted starting bromo-quinolone (0.68 g) and a solid which was recrystallised from ethyl acetate/methanol to afford the title compound, m.p. 306°-8°, (0.26 g), which was also confirmed spectroscopically to be identical to the product of Example 3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04740513
출처 데이터셋uspto-grants-1988_04
ORD IDord-fd88753c7fe748388fa3e1e6d2493b12
출처 메모uspto-grants-1988_04