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HRID 2394815作成日:2026年10月23日

(1S)-1-phenylpropan-1-amine → (S)-N-(alpha-Ethylbenzyl)-3-methyl-7-methoxy-2-phenylquinoline-4-carboxamide

https://huagongshe.com/ja/reaction/2394815

反応式

関与物質

役割名称HCID仕込み量
反応物(1S)-1-phenylpropan-1-amineHCID 6993773—
反応物3-Methyl-7-methoxy-2-phenylquinoline-4-carbonylchlorideHCID 22714324—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物(S)-N-(alpha-Ethylbenzyl)-3-methyl-7-methoxy-2-phenylquinoline-4-carboxamideHCID 53800998—

反応手順

Prepared as described in Ex. 1, starting from 1.27 g (4.09 mmol) of crude 3-methyl-7-methoxy-2-phenylquinoline-4-carbonylchloride, 0.55 g (4.09 mmol) of (S)-(-)-α-ethylbenzylamine and 1.71 ml (12.27 mmol) of TEA in 24 ml of dry CH2Cl2 and 1 ml of DMF to help solubility. The reaction mixture was stirred 12 hours at room temperature.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05811553
出典データセットuspto-grants-1998_09
ORD IDord-6a8cd2dc41ac4f62bcc83edbaf7232f5
出典メモuspto-grants-1998_09