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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1446676생성일: 2026년 10월 26일

Lithium Chloride → [4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-thiazol-2-ylmethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1446676

반응식

참여 물질

역할이름HCID투입량
반응물Lithium ChlorideHCID 433294—
반응물7-Chloro-3-iodoimidazo[1,2-a]pyridineHCID 57497697—
반응물(4-Trimethylstannyl-thiazol-2-ylmethyl)-carbamic acid tert-butyl esterHCID 66623970—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물[4-(7-Chloro-imidazo[1,2-a]pyridin-3-yl)-thiazol-2-ylmethyl]-carbamic acid tert-butyl esterHCID 6854596638.8%

반응 조건

온도90 °C

반응 단계

To a solution of (4-trimethylstannyl-thiazol-2-ylmethyl)-carbamic acid tert-butyl ester (0.480 g, 1.27 mmol, 1.0 eq.) [prepared as in the PCT application WO2004046101, Jun. 3, 2004, filed Nov. 10, 2003] in anhydrous dioxane (4 mL), add 7-chloro-3-iodo-imidazo[1,2-a]pyridine (0.354 g, 1.27 mmol, 1.0 eq.) and LiCl (0.162 g, 3.0 eq.). Add Pd(PPh3)4 (0.102 g, 0.07 eq.). Deoxygenate the reaction mixture and fill with nitrogen. Stir at 90° C. over night, cool, then dilute with 5% MeOH/DCM (100 mL), wash with saturated aqueous saturated sodium chloride (2×20 mL), water (2×20 mL), dry, filter, and concentrate. Chromatograph on silica gel first with a 50%-100% EtOAc/DCM gradient then a 5% MeOH/DCM gradient to afford 0.180 g of the title compound, which is used in the next step without further purification: MS(ES), m/z 365 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07666879B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-275102f6b24c4382811d7e18e5adea94
출처 메모uspto-grants-2010_02