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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1886377생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1886377

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물(S)-(-)-1-Amino-2-(methoxymethyl)pyrrolidineHCID 7156993—
반응물(+/-)-2-(3-Quinolinyl)cyclohexanoneHCID 19794569—
용매TolueneHCID 1140—
생성물(2S)-(-)-2-(methoxymethyl)-1-[2-(3-quinolinyl)cyclohexylideneamino]pyrrolidineHCID 57107142—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05151436
출처 데이터셋uspto-grants-1992_09
ORD IDord-bab73a4a228c43358d83afa5f35ad8c6
출처 메모uspto-grants-1992_09