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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 538427생성일: 2026년 10월 26일

Sodium Carbonate → 5-(2-(4-Fluorophenyl)thiazol-4-yl)-3-methoxypyridin-2-amine

https://huagongshe.com/reaction/538427

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물4-Bromo-2-(4-fluorophenyl)thiazoleHCID 45788231—
반응물3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 53398059—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-(2-(4-Fluorophenyl)thiazol-4-yl)-3-methoxypyridin-2-amineHCID 6659095488%

반응 단계

A mixture of 4-bromo-2-(4-fluorophenyl)thiazole (450 mg, 1.7 mmol), 3-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine (400 mg, 1.6 mmol), and aqueous 2.0 M Na2CO3 solution (2.3 mL, 4.6 mmol) in DME (6.8 mL) was sparged with Ar for 3 min. Tetrakis(triphenylphosphine)palladium(0) (120 mg, 0.1 mmol) was added and the reaction mixture was sparged with Ar for 1 min. The reaction was sealed and irradiated at 115° C. for 25 min in a microwave reactor. The reaction mixture was partitioned with EtOAc (50 mL) and saturated aqueous NaHCO3 solution (100 mL). The separated organic layer was washed with saturated aqueous NaHCO3 solution (50 mL). The organic layer was extracted with aqueous 0.5 N HCl solution (2×25 mL). The combined acidic aqueous portions were washed with EtOAc (30 mL), neutralized with saturated aqueous NaHCO3 solution and extracted with EtOAc (3×50 mL). The organic layer was dried (Na2SO4), filtered, and concentrated in vacuo. The crude material was purified by column chromatography over silica gel (SiO2, 100% EtOAc) to furnish 145 mg (88% purity) of 5-(2-(4-fluorophenyl)thiazol-4-yl)-3-methoxypyridin-2-amine which was directly used in the next step: LCMS (m/z): 302.1 (MH+), tR=0.75 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865732B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-bc56b03da8174e6d8666aa9ade278ac7
출처 메모uspto-grants-2014_10