돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 594897생성일: 2026년 10월 25일

Cesium carbonate → 6'-(3-Chloropyridin-2-yl)aminodispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetane]-2-amine

https://huagongshe.com/reaction/594897

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Amino-3-chloropyridineHCID 693267—
반응물Di-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
반응물Di-tert-butyl (6'-bromodispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-yl)imidodicarbonateHCID 86724239—
촉매(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one palladiumHCID 15673654—
용매1,4-DioxaneHCID 31275—
생성물6'-(3-Chloropyridin-2-yl)aminodispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetane]-2-amineHCID 8672429826.3%

반응 조건

온도100 °C

반응 단계

The mixture of di-tert-butyl (6′-bromodispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-yl)imidodicarbonate (150 mg, 0.286 mmol), 3-chloropyridin-2-amine (184 mg, 1.43 mmol), (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one-palladium (3:2) (52 mg, 0.057 mmol), di-tert-butyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (97 mg, 0.23 mmol), and Cs2CO3(279 mg, 0.857 mmol) in 1,4-dioxane (7.5 ml) was stirred for 48 hours at 100° C. The reaction mixture was cooled down to ambient temperature, and partitioned with CHCl3 and water. The organic layer was dried over Na2SO4, and filtered. The residue was dissolved in toluene, and was added silica gel (neutral), and stirred at 130° C. for 3 hours. The mixture was concentrated under reduced pressure, and purified by silica gel column chromatography (CHCl3/MeOH=100:0-85:15) to give an amorphous, which was washed with CHCl3/hexane to give 6′-(3-chloropyridin-2-yl)aminodispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetane]-2-amine (28 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242973B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-74e4cc55ff924317b0f8348615ee7db3
출처 메모uspto-grants-2016_01