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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 585367생성일: 2026년 10월 25일

1'-Benzylspiro[indoline-3,4'-piperidine] → 4-(1'-Benzylspiro[indoline-3,4'-piperidin]-1-yl)-1-(3,4-dimethoxybenzoyl)-2-methyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/585367

반응식

참여 물질

역할이름HCID투입량
반응물1'-Benzylspiro[indoline-3,4'-piperidine]HCID 16641028—
반응물cis-1-(3,4-Dimethoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinolHCID 69774154—
생성물4-(1'-Benzylspiro[indoline-3,4'-piperidin]-1-yl)-1-(3,4-dimethoxybenzoyl)-2-methyl-1,2,3,4-tetrahydroquinolineHCID 2233923552.4%

반응 단계

Starting with cis-1-(3,4-dimethoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol (400 mg, 1.22 mmol) prepared in Reference Example 1 and 1′-benzylspiro[indoline-3,4′-piperidine] (849 mg, 3.05 mmol), the same procedure as shown in Example 1 was repeated to give the titled compound (376 mg, yield: 44%) as a colorless oil. (cis:trans=1:1.5)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06930104B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-41b24b28573b4c52889c841e1d77e01b
출처 메모uspto-grants-2005_08