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HRID 851501作成日:2026年10月26日

3-(Trifluoromethyl)phenylglyoxal → N-(3-(4-Carbomethoxyphenyl)-1,1-dimethylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine

https://huagongshe.com/reaction/851501

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)phenylglyoxalHCID 2783284—
反応物Methyl 4-(3-amino-3-methylbutyl)benzoateHCID 20501354—
生成物N-(3-(4-Carbomethoxyphenyl)-1,1-dimethylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamineHCID 20501353—

反応手順

The title compound was prepared as in Example 1a from 3-trifluoromethylphenyl glyoxal (2.0 g) and 3-(4-carbomethoxyphenyl)-1,1-dimethylpropylamine (2.6 g) and isolated as the hydrochloride salt monohydrate m.p. 214°-219°. (methanol-ether). τ(DMSO d6) 8.6 (6H,s), 7.8-8.2 (2H,m), 6.6-7.4 (4H,m), 6.1 (3H,s), 5.8 (3H, broad, replaceable by D2O), 4.8 (1H,m), 2.55 (2H,d,J=8 Hz), 2.1-2.4 (4H,m), 2.07 (2H,d,J=8 Hz), 1.3 (1H, broad, replaceable by D2O), 0.33 (1H, broad, replaceable by D2O).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04385066
出典データセットuspto-grants-1983_05
ORD IDord-a6f25feab605470ea3374cce6f6bbb33
出典メモuspto-grants-1983_05