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HRID 460162作成日:2026年10月27日

Sodium cyanoborohydride → ((1R)-1-Phenylpropyl){[4-methoxy-3-(4-methoxyphenyl)phenyl]methyl}amine

https://huagongshe.com/reaction/460162

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium cyanoborohydrideHCID 5003444—
反応物(R)-1-PhenylpropylamineHCID 5324978—
反応物6,4'-Dimethoxybiphenyl-3-carbaldehydeHCID 22391191—
反応物(6,4'-Dimethoxybiphenyl-3-ylmethyl)-(1-quinolin-4-yl-ethyl)-amineHCID 22391337—
生成物((1R)-1-Phenylpropyl){[4-methoxy-3-(4-methoxyphenyl)phenyl]methyl}amineHCID 6001037052%

反応手順

The title compound was prepared by the same procedure for (6,4′-dimethoxy-biphenyl-3-ylmethyl)-(1-quinolin-4-yl-ethyl)-amine from (R)-(+)-1-phenyl-propylamine (405 mg, 3.0 mmol, Lancaster Synthesis Ltd.), 6,4′-Dimethoxy-biphenyl-3-carbaldehyde (242 mg, 1.0 mmol) and sodium cyanoborohydride (1.0 g, 16 mmol, Aldrich). The title compound was purified by column chromatography (silica gel, hexane/ethyl acetate 2/3) in form as white solid in 52% yield (187 mg, 0.52 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196102B2
出典データセットuspto-grants-2007_03
ORD IDord-746ec7ecabd448eb88e218169ac1c0ac
出典メモuspto-grants-2007_03