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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2236606생성일: 2026년 10월 26일

4-(Piperidin-1-ylmethyl)aniline → HCID 178484413, 화합물

https://huagongshe.com/reaction/2236606

반응식

참여 물질

역할이름HCID투입량
반응물4-(Piperidin-1-ylmethyl)anilineHCID 846150—
반응물4-Methoxymethylene-1,3-dioxo-1,2,3,4-tetrahydro-isoquinoline-6-carboxylic acid dimethylamideHCID 68699991—
용매DimethylformamideHCID 6228—
생성물HCID 178484413HCID 17848441374.7%

반응 단계

Prepared from a solution of 70 mg (0.255 mmol) of 4-methoxymethylene-1,3-dioxo-1,2,3,4-tetrahydro-isoquinoline-6-carboxylic acid dimethylamide and 48.5 mg (0.255 mmol) of 4-piperidin-1-ylmethyl-phenylamine in 1.6 mL of N,N-dimethylformamide (DMF) at 110° C. under N2 as described for example 21. After heating for 0.25 h, the reaction is chilled in ice. The solid product is collected, washed with N,N-dimethylformamide (DMF) and Et2O and dried to give 82.4 mg (74%) of bright yellow crystals: mp 266-267° C. (dec); 1H NMR (DMSO-d6) δ 12.45 (d, 1H, J=9 Hz), 11.40 (s, 1H), 8.95 (d, 1H, J=9 Hz), 8.17 (s, 1H), 8.06 (d, 1H, J=6 Hz), 7.53 (d, 2H, J=9 Hz), 7.32 (d, 2H, J=9 Hz), 7.20 (d, 1H, J=6 Hz), 3.42 (s, 2H), 3.04 (s, 3H), 2.90 (s, 3H), 2.32 (s, 4H), 1.48 (m, 4H), 1.38 (s, 2H); HRMS (ESI) m/e calcd for C25H28N4O3 431.20886, fond 431.20820 (M−H)−1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07713994B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-b6bd1d3a78974d8687414155444965c8
출처 메모uspto-grants-2010_05