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HRID 253115作成日:2026年10月24日

2-Bromopyridine → (+/-)-Ethyl 4-(pyridin-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate

https://huagongshe.com/ja/reaction/253115

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromopyridineHCID 7973—
反応物Cesium carbonateHCID 10796—
反応物Ethyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 31090—
反応物Binap, (A+-)-HCID 634876—
触媒Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物(+/-)-Ethyl 4-(pyridin-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylateHCID 8661401555.2%

反応条件

温度100 °C

反応手順

In a sealable tube, tris(dibenzylideneacetone) dipalladium (0) (5.2 mg, 0.0056 mmol), (S)-BINAP (10.7 mg, 0.017 mmol), cesium carbonate (132 mg, 0.41 mmol), 2-bromopyridine (33 □L, 0.35 mmol), and ethyl 3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate (Example 3a, 60 mg, 0.29 mmol) were dissolved in dioxane (2 mL). The reaction vessel was sealed and the suspension was heated at 100° C. for 20 h. The reaction mixture was cooled to ambient temperature, diluted with water (15 mL), and the product was extracted with dichloromethane (3×20 mL). The organic fractions were dried over sodium sulfate and concentrated. Purification of the product by flash column chromatography (15% to 25% EtOAc/hexane) afforded the title compound (46 mg, 0.16 mmol). MS m/z: 285 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872009B2
出典データセットuspto-grants-2011_01
ORD IDord-51e9447c75b04d669f08eb89eb40d763
出典メモuspto-grants-2011_01