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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51125생성일: 2026년 10월 26일

Sodium Hydroxide → 5-(4-(4-Phenoxyphenylamino)-quinolin-7-yl)thiazole-4-carbaldehyde

https://huagongshe.com/reaction/51125

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물(4-Phenoxyphenyl)-(7-iodoquinolin-4-yl)amineHCID 21952018—
반응물4-(1,3-Dioxolan-2-yl)-5-tributylstannylthiazoleHCID 21952069—
촉매Silver(II) oxideHCID 92152—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매Hydrochloric AcidHCID 313—
용매TetrahydrofuranHCID 8028—
생성물5-(4-(4-Phenoxyphenylamino)-quinolin-7-yl)thiazole-4-carbaldehydeHCID 5420401840.9%

반응 단계

Prepared according to Procedure B from (4-phenoxyphenyl)-(7-iodoquinolin-4-yl)amine (0.876 g, 2 mmol), 4-(1,3-dioxolan-2-yl)-5-tributylstannylthiazole (2.1 mmol), bis (triphenylphosphine) palladium (II) chloride (0.105 g, 0.15 mmol, 7.5 mol %) and silver oxide (0.463 g, 2 mmol) heated under reflux under nitrogen for 18 hr. The reaction mixture was then filtered through Harborlite® and the filtrate was concentrated. The product was purified on Bond Elut™ cartridge, eluting sequentially with dichloromethane, chloroform, diethyl ether and ethyl acetate. The ketal (0.385 g, 0.824 mmol) was stirred at room temperature in a mixture of THF (10 ml) and 1 N HCl (10 ml) for 2 hr. The suspension was basified with 2N NaOH (5 ml) and the THF was removed. The aqueous suspension was filtered and washed with water to give the product as a yellow solid (0.346 g);m/z 424.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713485B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-99a655602e0f4779a892e238c563e63b
출처 메모uspto-grants-2004_03