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HRID 73作成日:2026年10月23日

4-Aminobenzonitrile → HCID 178418220、化合物

https://huagongshe.com/ja/reaction/73

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminobenzonitrileHCID 13396—
反応物6-chloro-N-cyclohexylpyridine-3-carboxamideHCID 857493—
試薬Potassium tert-butoxideHCID 23665647—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,4-DioxaneHCID 31275—
生成物HCID 178418220HCID 1784182209.93%

反応条件

温度100 °C

反応手順

In a 50 mL round-bottomed flask a TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.115 g, 0.13 mmol),POTASSIUM TERT-BUTOXIDE (0.282 g, 2.51 mmol)and BINAP (0.157 g, 0.25 mmol) in dry 1,4-dioxane (10 mL) was mixed under N2.Followed by 6-chloro-N-cyclohexylnicotinamide (.300 g, 1.26 mmol) and 4-aminobenzonitrile (0.178 g, 1.51 mmol) was added and resulting mixture(dark brown) was heated at 100oC for 3 hrs.LCMS analysis showed the formation of required product.Reaction stopped,crude was passed through celite and washed with dioxane and finally with methanol.The filtrate was dried and dissolved in 3 ml DMSO for Waters MS Purification system.Pure fractions collected and concentrated.A White solid obtained as a product 6-(4-cyanophenylamino)-N-cyclohexylnicotinamide (0.040 g, 9.93 %).32 mg of above product was submitted for MGyrx2 projetct.LCMS/NMR confirmed the product.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-2d4104aef43247ff855d465ce3910528
出典メモ750 AstraZeneca ELN dataset