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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 519399생성일: 2026년 10월 26일

Sarcosine → 2-Bromo-6-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-trien-5-yl}benzaldehyde

https://huagongshe.com/reaction/519399

반응식

참여 물질

역할이름HCID투입량
반응물SarcosineHCID 1088—
반응물Potassium CarbonateHCID 11430—
반응물2,6-DibromobenzaldehydeHCID 12648641—
반응물6,7,8,9-Tetrahydrobenzo[4,5]thieno[2,3-d]pyridazin-4(3H)-oneHCID 67016553—
용매1,4-DioxaneHCID 31275—
생성물2-Bromo-6-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-trien-5-yl}benzaldehydeHCID 8668377760.1%

반응 조건

온도100 °C

반응 단계

A 25-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 1,4-dioxane (20 mL), 8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-trien-6-one 117c (618 mg, 3.0 mmol), 2,6-dibromobenzaldehyde (1980 mg, 7.5 mmol), CuBr (215 mg, 1.5 mmol), sarcosine (267 mg, 3.0 mmol), and K2CO3 (828 mg, 6.0 mmol). After three cycles of vacuum/argon flush, the mixture was heated at 100° C. for 16 h. After this time the reaction was cooled to room temperature. It was then filtered and the filtrate was evaporated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with 30:1 dichloromethane/methanol to afford 130a (702 mg, 60%) as a yellow solid. MS: [M+H]+ 389.0

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115152B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-d6c6500de8a541c6a23147b9011ad863
출처 메모uspto-grants-2015_08