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HRID 226071作成日:2026年10月25日

8-(1-Ethyl-propyl)-3-iodo-2,6-dimethyl-imidazo[1,2-b]pyridazine → 8-(1-Ethyl-propyl)-2,6-dimethyl-3-(2-methyl-thieno[2,3-b]pyridin-3-yl)-imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/226071

反応式

関与物質

役割名称HCID仕込み量
反応物8-(1-Ethyl-propyl)-3-iodo-2,6-dimethyl-imidazo[1,2-b]pyridazineHCID 57752681—
反応物3-Bromo-2-methylthieno(2,3-b)pyridineHCID 68857726—
触媒ZincHCID 23994—
溶媒TetrahydrofuranHCID 8028—
生成物8-(1-Ethyl-propyl)-2,6-dimethyl-3-(2-methyl-thieno[2,3-b]pyridin-3-yl)-imidazo[1,2-b]pyridazineHCID 5775264110.4%

反応条件

温度100 °C

反応手順

382 mg of 3-Bromo-2-methyl-thieno[2,3-b]pyridine (1.67 mmol) is placed into the vial with 2.5 ml of Reiki Zn, suspension in THF (1.75 mmol) and capped and heated at 100° C. for 2 h. The excess Zinc is allowed to settle down and the solution is transferred to the vial containing 200 mg of 8-(1-ethyl-propyl)-3-iodo-2,6-dimethyl-imidazo[1,2-b]pyridazine (0.58 mmol) and 41 mg of PdCl2(pddf) (0.05 mmol) in 3 ml of dry THF. The vial is capped with a Teflon cap and heated at 80° C. for 2 days. The reaction mixture is quenched with sat. NH4Cl and extracted by CH2Cl2, dried over Na2SO4 and evaporated. The crude product is applied onto a silica-gel chromatography column (Hexane:AcOEt=8:1) to give 22 mg of the title compound. Yield 4%. mass spectrum (m/e): 365 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557103B2
出典データセットuspto-grants-2009_07
ORD IDord-18e3f1ab9d99438a991b30b2471e11d5
出典メモuspto-grants-2009_07