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HRID 534002作成日:2026年10月25日

Water → (R)-1-(2-(5-bromo-3-(4-fluorophenoxy)pyridin-2-ylamino)thiazol-4-yl)ethane-1,2-diol

https://huagongshe.com/reaction/534002

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-(5-Bromo-3-(4-fluorophenoxy)pyridin-2-yl)thioureaHCID 86631485—
反応物(S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanoneHCID 86644148—
溶媒EthanolHCID 702—
生成物(R)-1-(2-(5-bromo-3-(4-fluorophenoxy)pyridin-2-ylamino)thiazol-4-yl)ethane-1,2-diolHCID 594437197%

反応条件

温度80 °C

反応手順

To 1-(5-bromo-3-(4-fluorophenoxy)pyridin-2-yl)thiourea (0.5 g, 1.5 mmol) in ethanol (50 mL) was added (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone (0.34 g, 1.9 mmol) and the reaction stirred at 80° C. for 1 hr. The reaction was poured into water (250 mL) and then filtered. The solid was triturated with ethyl acetate and methanol. The solid was suspended in ethyl acetate (500 mL) and washed with 1 N NaOH (500 mL). The organics were concentrated and the crude material was purified by chromatography using 3 to 10% MeOH/CH2Cl2 as eluent to give (R)-1-(2-(5-bromo-3-(4-fluorophenoxy)pyridin-2-ylamino)thiazol-4-yl)ethane-1,2-diol (0.043 g, 0.10 mmol, 7%) (ABCI POS 426, 428 M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853409B2
出典データセットuspto-grants-2014_10
ORD IDord-11d7b316fd614627bc2742dfaa08392b
出典メモuspto-grants-2014_10