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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 873757생성일: 2026년 10월 25일

Sodium Carbonate → 6'-(4-Methoxypyridin-2-yl)-2',2'-dimethyldispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-amine

https://huagongshe.com/reaction/873757

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Bromo-4-methoxypyridineHCID 4738484—
반응물Di-tert-butyl[2',2'-dimethyl-6'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)dispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-yl]imidodicarbonateHCID 86724310—
촉매HCID 178418397HCID 178418397—
용매Chloroform methanolHCID 21584188—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물6'-(4-Methoxypyridin-2-yl)-2',2'-dimethyldispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-amineHCID 8672430981.4%

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온도100 °C

반응 단계

A mixture of di-tert-butyl [2′,2′-dimethyl-6′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)dispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-yl]imidodicarbonate (282 mg, 0.470 mmol), 2-bromo-4-methoxypyridine (221 mg, 1.17 mmol), tetrakis(triphenylphosphine)palladium(0) (271 mg, 0.235 mmol) and Na2CO3 (149 mg, 1.41 mmol) in dioxane-water (4:1, 5.6 mL) was stirred for 8 hours at 100° C. The mixture was diluted with MeOH—CHCl3 (1:9) and washed with water, then the organic layer was dried over MgSO4 and filtered. The filtrate was concentrated at reduced pressure. To the residue were added toluene (2.8 mL) and silica gel (neutral; 846 mg), and the mixture was stirred for 3 hours at 120° C. After concentration of the reaction mixture at reduced pressure, the residue was purified with column chromatography on silica gel (CHCl3-EtOH, a linear gradient of EtOH from 0 to 20%) afforded 6′-(4-methoxypyridin-2-yl)-2′,2′-dimethyldispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-amine (146 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975415B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-828ea07df72643b789eecff679ccedaf
출처 메모uspto-grants-2015_03