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HRID 602417作成日:2026年10月25日

Toluene → N-(2-methyl-2H-indazol-6-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide

https://huagongshe.com/reaction/602417

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2-Methyl-2H-indazol-6-amineHCID 590220—
反応物Potassium sodium tartarateHCID 9855836—
反応物TrimethylaluminumHCID 16682925—
反応物2-{[2-(3-Methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinic acid methyl esterHCID 58674945—
溶媒1,2-DichloroethaneHCID 11—
生成物N-(2-methyl-2H-indazol-6-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamideHCID 1161170953%

反応条件

温度85 °C

反応手順

A suspension of 2-methyl-2H-indazol-6-ylamine [Davies J. Chem. Soc.; 1955; 2412-2419] (809 mg, 5.5 mmol) in DCE (13.5 mL) was treated at 0° C. consecutively with, trimethylaluminium (2 M) in toluene (4.23 mL, 8.46 mmol), 2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinic acid methyl ester (1.34 g, 4.23 mmol) and DCE (20 mL). The reaction mixture was placed under a nitrogen atmosphere and heated for 10 hours at 85° C. (bath temperature). On cooling the reaction was poured into aqueous sodium-potassium tartrate solution (150 mL) and partitioned between EtOAc and water. The organic phase was washed with brine, dried, filtered and concentrated in vacuo. The residue was purified by chromatography on silica gel (Gradient elution: 100% CH2Cl2 to 90% CH2Cl2/10% MeOH) to give N-(2-methyl-2H-indazol-6-yl)-2-{[2-(3-methyl-ureido)-pyridin-4-ylmethyl]-amino}-nicotinamide (964 mg, 53%) as a solid; Mp. 205-207° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906533B2
出典データセットuspto-grants-2011_03
ORD IDord-d2ef29d827fd4511b2b807b41a627d4d
出典メモuspto-grants-2011_03