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HRID 519399作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物SarcosineHCID 1088—
反応物Potassium CarbonateHCID 11430—
反応物2,6-DibromobenzaldehydeHCID 12648641—
反応物6,7,8,9-Tetrahydrobenzo[4,5]thieno[2,3-d]pyridazin-4(3H)-oneHCID 67016553—
溶媒1,4-DioxaneHCID 31275—
生成物2-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%

反応条件

温度100 °C

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115152B2
出典データセットuspto-grants-2015_08
ORD IDord-d6c6500de8a541c6a23147b9011ad863
出典メモuspto-grants-2015_08