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HRID 394733作成日:2026年10月24日

Pyridine → N-[4-[(3-chlorophenyl)amino]quinazolin-6-yl]acrylamide hydrochloride

https://huagongshe.com/ja/reaction/394733

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物N4-(3-chlorophenyl)quinazoline-4,6-diamineHCID 11807783—
反応物Ethylcarbodiimide hydrochlorideHCID 21883477—
反応物tetrahydrofuran N,N-dimethylformamideHCID 21974620—
生成物N-[4-[(3-chlorophenyl)amino]quinazolin-6-yl]acrylamide hydrochlorideHCID 1817623748%

反応条件

温度0 °C

反応手順

1-3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1902 mg, 1 mmol) was added to a solution of 6-amino-4[(3-chlorophenyl)amino]quinazoline (136 mg, 0.5 mmol) acrylic acid (74 mg, 1.0 mmol) and pyridine (201 mg, 2.5 mmol) in THF/DMF (4:1, 2.5 mL), stirred under nitrogen at 0° C. After 20 minutes the reaction mixture was stirred at 25° C. for 3 hours, and then poured onto water (12.5 mL), and extracted with EtOAc (2×10 mL). The combined extracts were treated with dilute hydrochloric acid (0.5 M, 10 mL), and the precipitate was collected by Buchner filtration, rinsed with water (10 mL), ether (2×10 mL), and air dried to give N-[4-[(3-chlorophenyl)amino]quinazolin-6-yl]acrylamide hydrochloride (93 mg, 48%) as a dull yellow solid, mp 223-227° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06602863B1
出典データセットuspto-grants-2003_08
ORD IDord-b0e20fda70b94efb95f3316988b28dbd
出典メモuspto-grants-2003_08