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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219987생성일: 2026년 10월 25일

3-(Methoxymethyl)-4-(2-methylpiperidin-1-yl)benzoic acid → HCID 67529400, 화합물

https://huagongshe.com/reaction/219987

반응식

참여 물질

역할이름HCID투입량
반응물3-(Methoxymethyl)-4-(2-methylpiperidin-1-yl)benzoic acidHCID 59495804—
반응물HCID 72307492HCID 72307492—
생성물HCID 67529400HCID 67529400—

반응 단계

The title compound was prepared following procedure described for example 141, step 1, but starting from Intermediate 58 (158 mg; 0.60 mmol) and Intermediate 67 (151.79 mg; 0.57 mmol), the crude mixture was purified by flash chromatography (c-hex/(DCM/EtOAc 1:1) gradient from 1:0 to 1:1) to afford the title compound as a colorless oil. 1H NMR (CDCl3) δ 8.32 (d, J=2.1 Hz, 1H), 8.09 (dd, J=8.2, 2.1 Hz, 1H), 7.77 (dd, J=7.7, 1.2 Hz, 1H), 7.69 (dd, J=2.5, 1.4 Hz, 1H), 7.40 (t, J=8.0 Hz, 1H), 7.26 (d, J=8.3 Hz, 1H), 7.04 (ddd, J=8.3, 2.6, 0.9 Hz, 1H), 4.68-4.57 (m, 2H), 4.20-4.09 (m, 4H), 3.49 (s, 3H), 3.16 (br s, 1H), 3.06-3.02 (m, 1H), 2.65-2.62 (m, 1H), 2.56 (t, J=7.3 Hz, 2H), 2.20-2.11 (m, 2H), 1.86-1.69 (m, 4H), 1.49-1.45 (m, 2H), 1.27 (t, J=7.2 Hz, 3H), 0.89 (d, J=6.2 Hz, 3H). LC/MS (Method B): 494.5 (M+H)+. HPLC (Method A) Rt 4.59 min (Purity: 98.9%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202865B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-5abd944d549a4d0bbeccb17ae133b6e6
출처 메모uspto-grants-2012_06