돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1177532생성일: 2026년 10월 25일

Sulfoxonium, trimethyl-, iodide (1:1) → 2-(4-(1,3-dioxan-2-yl)-2-fluorophenyl)-5-(1-(tetrahydro-2H-pyran-4-yl)cyclopropyl)thiazolo[5,4-b]pyridine

https://huagongshe.com/reaction/1177532

반응식

참여 물질

역할이름HCID투입량
반응물Sulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-(4-(1,3-dioxan-2-yl)-2-fluorophenyl)-5-(1-(tetrahydro-2H-pyran-4-yl)vinyl)thiazolo[5,4-b]pyridineHCID 67112136—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
생성물2-(4-(1,3-dioxan-2-yl)-2-fluorophenyl)-5-(1-(tetrahydro-2H-pyran-4-yl)cyclopropyl)thiazolo[5,4-b]pyridineHCID 67111805—

반응 조건

온도60 °C

반응 단계

To a slurry of 2-(4-(1,3-dioxan-2-yl)-2-fluorophenyl)-5-(1-(tetrahydro-2H-pyran-4-yl)vinyl)thiazolo[5,4-b]pyridine (0.201 g, 0.471 mmol) in 2.5 mL THF was added a solution of trimethylsulfoxonium iodide (0.207 g, 0.943 mmol) and potassium tert-butoxide (0.106 g, 0.943 mmol) in 2.5 mL DMSO. The yellow slurry was sealed and heated to 60° C. After 6 h, the reaction mixture was cooled, quenched with ice and sat'd aq. NH4Cl. The reaction mixture was partitioned between satd aq NH4Cl and DCM. The aqueous layer was extracted with DCM 3 times, and the combined organics were dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The material was purified by silica gel chromatography, 0-50% EA/hexanes, to give 2-(4-(1,3-dioxan-2-yl)-2-fluorophenyl)-5-(1-(tetrahydro-2H-pyran-4-yl)cyclopropyl)thiazolo[5,4-b]pyridine as a solid. MS (ESI) m/z: Calculated: 440.2; Observed: 441.1 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07842685B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-becbb258c0cb47ffa138fd19f33ce495
출처 메모uspto-grants-2010_11