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HRID 1160127作成日:2026年10月23日

O-Xylene → Imatinib

https://huagongshe.com/ja/reaction/1160127

反応式

関与物質

役割名称HCID仕込み量
反応物O-XyleneHCID 7237—
反応物Binap, (A+-)-HCID 634876—
反応物N-(3-bromo-4-methyl-phenyl)4-(4-methyl-piperazin-1-ylmethyl)-benzamideHCID 10309714—
反応物4-(Pyridin-3-yl)pyrimidin-2-amineHCID 12450582—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒WaterHCID 962—
生成物ImatinibHCID 5291—

反応手順

To a mixture of 4-(3-pyridyl)-2-pyrimidine-amine (172.2 mg, 1.0 mmol), N-(3-bromo-4-methyl-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide (402.4 mg, 1.0 mmol) and sodium tert.-butylate (144.2 mg, 1.5 mmol) is added a mixture of rac-BINAP (31.2 mg, 0.050 mmol) and Pd2(dba)3*CHCl3 (13 mg, 0.013 mmol) under argon. After addition of 3 ml of xylene the suspension is sonicated for 10 minutes then stirred for 5 hours under reflux. After cooling to room temperature, water (10 ml) is added to the dark brown oil and the product extracted 4 times with methylene chloride (10 ml each). The combined organic extracts are dried over MgSO4 and concentrated in vacuo. The brown oil is purified by flash-chromatography (SiO2, methanol). The product, a pale yellow solid is dissolved in methylene chloride, filtered and concentrated in vacuo. Yield: 484.3 mg of the title compound, 72% of theory, (99.9% area by HPLC). The product contains typically roughly 10% of isomers which can be eliminated by preparative reversed phase chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816359B2
出典データセットuspto-grants-2010_10
ORD IDord-214efff2b2f54554ba7e8db81d7bc8d6
出典メモuspto-grants-2010_10