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HRID 1886377作成日:2026年10月27日

p-Toluenesulfonic acid → (2S)-(-)-2-(methoxymethyl)-1-[2-(3-quinolinyl)cyclohexylideneamino]pyrrolidine

https://huagongshe.com/reaction/1886377

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物(S)-(-)-1-Amino-2-(methoxymethyl)pyrrolidineHCID 7156993—
反応物(+/-)-2-(3-Quinolinyl)cyclohexanoneHCID 19794569—
溶媒TolueneHCID 1140—
生成物(2S)-(-)-2-(methoxymethyl)-1-[2-(3-quinolinyl)cyclohexylideneamino]pyrrolidineHCID 57107142—

反応手順

A mixture of (±)-2-(3-quinolinyl)cyclohexanone (0.5 g, 2.2 mmol), (S)-(-)-1-amino-2-(methoxymethyl)pyrrolidine (`SAMP`)(0.28 g, 2.2 mmol) and p-toluenesulphonic acid (10 mg) was refluxed in toluene (15 ml) for 2.5 hours. The toluene was removed in vacuo (40° C./14 mmHg,) to give a crude oil which was partitioned between water (20 ml) and ethyl acetate (25 ml). The aqueous layer was extracted with ethyl acetate (2×25 ml) and the combined organic extracts were dried over sodium sulphate then concentrated in vacuo to give (2S)-(+)-2-(methoxymethyl) -1-[2-(3-quinolinyl)cyclohexylideneamino]pyrrolidine and (2S)-(-)-2-(methoxymethyl)-1-[2-(3-quinolinyl)cyclohexylideneamino]pyrrolidine as a 50:50 mixture of diastereoisomers (0.69 g, 2 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05151436
出典データセットuspto-grants-1992_09
ORD IDord-bab73a4a228c43358d83afa5f35ad8c6
出典メモuspto-grants-1992_09