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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253115생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-BromopyridineHCID 7973—
반응물Cesium carbonateHCID 10796—
반응물Ethyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 31090—
반응물Binap, (A+-)-HCID 634876—
촉매Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물(+/-)-Ethyl 4-(pyridin-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylateHCID 8661401555.2%

반응 조건

온도100 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872009B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-51e9447c75b04d669f08eb89eb40d763
출처 메모uspto-grants-2011_01