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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1832229생성일: 2026년 10월 26일

9-ethyl-9H-carbazole-3-carbaldehyde → N-(3-{1-[(9-ethyl-9H-carbazol-3-yl)methyl]-4-piperidinyl)phenyl)-2-methylpropanamide

https://huagongshe.com/reaction/1832229

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참여 물질

역할이름HCID투입량
반응물9-ethyl-9H-carbazole-3-carbaldehydeHCID 82055—
반응물N-(3-{1-[4-(4-chlorophenoxy)benzyl]-4-piperidinyl}phenyl)-2-methylpropanamideHCID 16756642—
반응물2-methyl-N-[3-(4-piperidyl)phenyl]propanamideHCID 16757255—
반응물N-(4-{1-[(9-ethyl-9H-carbazol-3-yl)methyl]-4-piperidinyl}phenyl)-2-methylpropanamideHCID 22048899—
생성물N-(3-{1-[(9-ethyl-9H-carbazol-3-yl)methyl]-4-piperidinyl)phenyl)-2-methylpropanamideHCID 1013900795%

반응 단계

According to the procedure used for the synthesis of N-(3-{1-[4-(4-CHLOROPHENOXY)BENZYL]-4-PIPERIDINYL}PHENYL)-2-METHYLPROPANAMIDE (Example 108) N-(4-{1-[(9-ethyl-9H-carbazol-3-yl)methyl]-4-piperidinyl}phenyl)-2-methylpropanamide, 9-ethyl-9H-carbazole-3-carbaldehyde and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide afforded N-(3-{1-[(9-ethyl-9H-carbazol-3-yl)methyl]-4-piperidinyl}phenyl)-2-methylpropanamide (37 mg, 95%). 1H NMR (400 MHz, CDCl3) δ 8.24–6.29 (m, 12H), 4.37 (q, 2H, J=7.2 Hz), 3.82 (s, 2H), 3.23–3.06 (m, 2H), 2.65–2.38 (m, 2H), 2.31–2.11 (m, 2H), 2.01–1.73 (m, 4H), 1.43 (t, 3H, J=7.2 Hz), 1.25 (d, 6H, J=4.0 Hz); ESMS m/e: 454.3 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07067534B1
출처 데이터셋uspto-grants-2006_06
ORD IDord-daa084a95b844a4499fe2ea172cdd01d
출처 메모uspto-grants-2006_06