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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538425생성일: 2026년 10월 26일

Potassium Carbonate → 3-Methoxy-5-(2-phenyl-4-(pyridin-4-yl)thiazol-5-yl)pyridin-2-amine

https://huagongshe.com/reaction/538425

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 53398059—
반응물5-Bromo-2-phenyl-4-(pyridin-4-yl)thiazoleHCID 66590540—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물3-Methoxy-5-(2-phenyl-4-(pyridin-4-yl)thiazol-5-yl)pyridin-2-amineHCID 59137604—

반응 단계

A mixture of 5-bromo-2-phenyl-4-(pyridin-4-yl)thiazole (20 mg, 0.062 mmol), 3-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine (39 mg, 0.157 mmol), and aqueous 2.0 M K2CO3 solution (0.5 ml, 1 mmol) in dioxane (0.5 mL) was sparged with Ar. Pd(PPh3)4 (181 mg, 0.157 mmol) was added, the reaction was sealed and irradiated at 120° C. for 15 min. While allowing to cool to rt, the reaction partitioned and the resulting layers were separated. The aqueous phase was extracted with EtOAc (3×) and the combined organic phases were washed with brine, dried (Na2SO4), and concentrated. The resulting residue was purified by reverse phase HPLC to give, after freeze drying, 3-methoxy-5-(2-phenyl-4-(pyridin-4-yl)thiazol-5-yl)pyridin-2-amine as the TFA salt: LCMS (m/z): 361.0 (MH+), tR=0.58 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865732B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-b1ec43678c014042ad82e9af5f9403ca
출처 메모uspto-grants-2014_10