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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1832230생성일: 2026년 10월 26일

4-Iodoanisole → N-[3-(1-{[1-(4-Methoxyphenyl)-1H-indol-5-YL]methyl}-4-piperidinyl)phenyl]-2-methylpropanamide

https://huagongshe.com/reaction/1832230

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참여 물질

역할이름HCID투입량
반응물4-IodoanisoleHCID 69676—
반응물N-(4-methylphenyl)indoleHCID 9794286—
반응물N-{3-[1-(1H-indol-5-ylmethyl)-4-piperidinyl]phenyl)-2-methylpropanamideHCID 22049334—
생성물N-[3-(1-{[1-(4-Methoxyphenyl)-1H-indol-5-YL]methyl}-4-piperidinyl)phenyl]-2-methylpropanamideHCID 2204940956.1%

반응 단계

According to the procedure used for the synthesis of 1-(4-methylphenyl)1H-indole, N-{3-[1-(1H-indol-5-ylmethyl)-4-piperidinyl]phenyl}-2-methylpropanamide (37.5 mg, 0.100 mmol) and 1-iodo-4-methoxybenzene (46.8 mg, 0.200 mmol) gave the desired product (27 mg, 56%). 1H NMR (400 MHz, CDCl3) δ 7.70–6.58 (m, 14H), 3.88 (s, 3H), 3.67 (s, 2H), 3.14–3.01 (m, 2H), 2.57–2.41 (m, 2H), 2.25–2.01 (m, 2H), 1.93–1.69 (m, 4H), 1.24 (d, 6H, J=7.2 Hz); ESMS m/e: 482.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07067534B1
출처 데이터셋uspto-grants-2006_06
ORD IDord-a6fd79f82bb248b28b9a25fc8204e6b9
출처 메모uspto-grants-2006_06