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HRID 9458作成日:2026年10月24日

Triethylamine → 1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol

https://huagongshe.com/ja/reaction/9458

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Propanol, 1-amino-2-methyl-HCID 95102—
反応物7-Benzyl-4-chloro-3-nitroquinolineHCID 21984193—
反応物6-Benzyl-4-chloro-3-nitroquinolineHCID 21984226—
溶媒DichloromethaneHCID 6344—
生成物1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-olHCID 21984410—
生成物1-(7-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-olHCID 21984452—

反応手順

Under a nitrogen atmosphere, 1-amino-2-methylpropan-2-ol (1.2 equivalents) was added to a 0.2 M solution of 7-benzyl-4-chloro-3-nitroquinoline or 6-benzyl-4-chloro-3-nitroquinoline (1 equivalent) and triethylamine (3 equivalents) in dichloromethane, and the reaction was stirred overnight at ambient temperature. The volatiles were removed under reduced pressure, and the residue was stirred with water (50 mL) for one hour. The resulting yellow solid was isolated by filtration and washed with water to provide 1-(7-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol or 1-(6-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol, respectively.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091214B2
出典データセットuspto-grants-2006_08
ORD IDord-a26247a753df407cb8aa5733bcc350c4
出典メモuspto-grants-2006_08