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HRID 855307作成日:2026年10月24日

3,4-Dichlorophenethylamine → [3-Chloro-4-(1-methylcyclopropyl)-benzyl]-[2-(3,4-dichlorophenyl)-ethyl]-amine

https://huagongshe.com/ja/reaction/855307

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-DichlorophenethylamineHCID 217958—
反応物Sodium borohydrideHCID 4311764—
反応物(4-Cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amineHCID 69342889—
反応物HCID 86093823HCID 86093823—
生成物[3-Chloro-4-(1-methylcyclopropyl)-benzyl]-[2-(3,4-dichlorophenyl)-ethyl]-amineHCID 6934210899%

反応手順

The title compound was synthesized in analogy to (4-cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amine (described in example S53) using 3-chloro-4-(1-methylcyclopropyl)-benzaldehyde (prepared as described in example S105) (90 mg, 0.46 mmol), 2-(3,4-dichlorophenyl)-ethylamine (88 mg, 0.46 mmol) and sodium borohydride (26 mg, 0.70 mmol). The desired product (168 mg, 99%) was isolated without further purification as a colorless oil. MS (ISP) 370.1 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07259183B2
出典データセットuspto-grants-2007_08
ORD IDord-3d83317f05dc4ddea6963a9401a9b144
出典メモuspto-grants-2007_08