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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1879673생성일: 2026년 10월 24일

Cesium carbonate → 2-Bromo-6-(8-tert-butyl-5-oxo-1,2,3,5-tetrahydrobenzo[e][1,4]diazepin-4-yl)-benzaldehyde

https://huagongshe.com/ko/reaction/1879673

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물2,6-DibromobenzaldehydeHCID 12648641—
반응물8-tert-Butyl-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-oneHCID 59548532—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
용매1,4-DioxaneHCID 31275—
생성물2-Bromo-6-(8-tert-butyl-5-oxo-1,2,3,5-tetrahydrobenzo[e][1,4]diazepin-4-yl)-benzaldehydeHCID 59548536—

반응 조건

온도100 °C

반응 단계

8-tert-Butyl-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one (420 mg, 2 mmol), 2,6-Dibromo-benzaldehyde (2.03 g, 8 mmol, 3eq), Xanthphos (22 mg, 0.02eq), and cesium carbonate (1.23 g, 4 mmol, 2 eq) were taken up in dioxane (5.0 mL) and a stream of argon gas was bubbled through the mixture for 1 minute. The catalyst Pd(dba)2 (33 mg, 0.03 eq) was added and argon was bubbled through for an additional minute. The resulting mixture was sealed under argon and stirred at 100° C. for 18 hours. The reaction was cooled and filtered. The collected solid was triturated with water and filtered to give a solid. The dioxane filtrate was combined with this solid, the solvent removed under vacuum, and the residue chromatographed, eluting with 50% ethyl acetate in hexanes gave a solid, 81 mg. (M+H)+=402.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08318719B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-ed7acf2dedb64cccaed3e5bd00607747
출처 메모uspto-grants-2012_11