戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 133437作成日:2026年10月26日

Methanamine, N-methoxy-, hydrochloride (1:1) → N-Methoxy-N-methyl-3-(4-chlorophenyl)-2-(3-fluorophenyl)propanamide

https://huagongshe.com/reaction/133437

反応式

関与物質

役割名称HCID仕込み量
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物Methyl 3-(4-chlorophenyl)-2-(3-fluorophenyl)propionateHCID 16098347—
反応物Dimethylalumanylium chlorideHCID 16686359—
溶媒DichloromethaneHCID 6344—
生成物N-Methoxy-N-methyl-3-(4-chlorophenyl)-2-(3-fluorophenyl)propanamideHCID 16098351—

反応手順

To a suspension N-methoxy-N-methylamine hydrochloride (2.0 g, 21 mmol) in 50 mL CH2Cl2 at 0° C. was added dimethylaluminum chloride (1 M in hexane, 21 mL, 21 mmol). After stirring at room temperature for 1 h, a solution of methyl 3-(4-chlorophenyl)-2-(3-fluorophenyl)propionate (Step A, 2.0 g, 10 mmol) in CH2Cl2 (10 mL) was added, and the resulting mixture was stirred overnight. The reaction mixture was quenched by addition of MeOH (5 mL), and the resulting mixture was concentrated with silica gel (50 g). The material was loaded onto a silica gel column, which was eluted with 10% EtOAc in hexane to 2% ammonia in MeOH (2 M) in 10% EtOAc/hexane to give the title compound. 1H NMR (400 MHz, CD3OD): δ 7.35-6.90 (m, 8H), 4.39 (br, 1H), 3.41 (s, 3H), 3.38-3.30 (m, 1H), 3.08 (s, 3H), 2.92 (dd, 1H). LC-MS: m/e 322 (M+H)+ (3.6 min).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390835B2
出典データセットuspto-grants-2008_06
ORD IDord-bdb3a302d9924d91aa890ebc3c4f8da6
出典メモuspto-grants-2008_06