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HRID 335269作成日:2026年10月25日

2-Methylpentane → 7-Bromo-N-(2-methyl-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/335269

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylpentaneHCID 7892—
反応物2-(4-Methyl-1-piperazinyl)benzenemethanamineHCID 2795568—
反応物Methyl 3-(7-bromoimidazo[1,2-a]pyridine-3-carboxamido)-4-methylbenzoateHCID 71283103—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物7-Bromo-N-(2-methyl-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 71283107—

反応条件

温度100 °C

反応手順

Methyl 3-(7-bromoimidazo[1,2-a]pyridine-3-carboxamido)-4-methylbenzoate (Intermediate 1B) (400 mg, 1.030 mmol) and TBD (143 mg, 1.030 mmol) in toluene (10 ml) was treated with (2-(4-methylpiperazin-1-yl)phenyl)methanamine (212 mg, 1.030 mmol) and heated at 100° C. under nitrogen overnight. Further TBD (106 mg, 0.82 mmol) was added the mixture was heated at 100° C. for a further 24 hrs. The solvent was removed in vacuo and the residue was partitioned between EtOAc (50 ml) and sodium bicarbonate solution (50 ml). The organic portion was separated and washed with sodium bicarbonate (2×25 ml), dried (MgSO4), filtered and evaporated to dryness to give a yellow solid. Purification by chromatography on silica eluting with 0-20% 2M NH3 in MeOH/DCM afforded a colourless oil. The oil was dissolved in minimum volume of EtOAc and titurated iso-hexane to afford the title compound as a white solid;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883819B2
出典データセットuspto-grants-2014_11
ORD IDord-4fe692db07194191a3b9e2b5dc83a22a
出典メモuspto-grants-2014_11