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HRID 1676324作成日:2026年10月26日

1,2-Dimethoxyethane → (4-(7-(4-Amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)phenyl)(morpholino)methanone

https://huagongshe.com/reaction/1676324

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物Cesium carbonateHCID 10796—
反応物[4-(Morpholine-4-carbonyl)phenyl]boronic acidHCID 2773546—
反応物3-Fluoro-4-((2-iodothieno[3,2-b]pyridin-7-yl)oxy)anilineHCID 58474950—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物(4-(7-(4-Amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)phenyl)(morpholino)methanoneHCID 6734726513.3%

反応条件

温度85 °C

反応手順

A sealable tube was charged with 3-fluoro-4-(2-iodothieno[3,2-b]pyridin-7-yloxy)aniline (Example 6, Step A, 0.200 g, 0.518 mmol), cesium carbonate (0.253 g, 0.777 mmol), 4-(morpholine-4-carbonyl)phenylboronic acid (0.183 g, 0.777 mmol) and DME (2 mL). The mixture was degassed under nitrogen for 10 minutes and Pd(PPh3)4 (0.0299 g, 0.0259 mmol) was added as a solid. The mixture was heated to 85° C. for 18 hours. The crude was diluted with water (300 mL), extracted with EtOAc/MeOH (4:1, 2×300 mL), dried organic over sodium sulfate, filtered and concentrated. The crude product was purified by preparative TLC (2.0 mm thickness) eluting with EtOAc/MeOH (9:1) to give product (31 mg, 12%) as a white solid. LRMS (APCI+) 450 m/z (M+1) detected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08003662B2
出典データセットuspto-grants-2011_08
ORD IDord-a7094c19d4d347a49b907ffef16ad68e
出典メモuspto-grants-2011_08