戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1091619作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/1091619

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4-Bromo-2-(4-fluorophenyl)thiazoleHCID 45788231—
反応物3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 53398059—
触媒HCID 178418397HCID 178418397—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物5-(2-(4-Fluorophenyl)thiazol-4-yl)-3-methoxypyridin-2-amineHCID 6659095488%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129394B2
出典データセットuspto-grants-2012_03
ORD IDord-87cfb540a92c4bf29864e25cf69ff54a
出典メモuspto-grants-2012_03