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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 749729생성일: 2026년 10월 26일

Ammonia → 1-Benzyl-3-(3-chloro-phenyl)-5-methyl-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine

https://huagongshe.com/reaction/749729

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물BenzylamineHCID 7504—
반응물Ethyl 4-oxo-1-piperidinecarboxylateHCID 34767—
반응물1-Chloro-3-(2-nitroethenyl)benzeneHCID 2731646—
용매Ethylacetate methanolHCID 21584119—
생성물1-Benzyl-3-(3-chloro-phenyl)-5-methyl-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridineHCID 59752511—

반응 단계

The title compound (0.34 g) was prepared from 3.0 g of 4-oxo-piperidine-1-carboxylic acid ethyl ester, 1.91 mL of benzylamine, and 1.2 g of 1-chloro-3-(2-nitro-vinyl)-benzene as in Example 38. TLC (SiO2, 2% NH3 in MeOH/EtOAc): Rf=0.25. MS (ESI): exact mass calculated for C21H21ClN2, 336.14; found, m/z 337.2 [M+H]+, 339.2 [M+H]+. 1H NMR (500 MHz, CD3OD): 7.36-7.32 (m, 4H), 7.30-7.25 (m, 2H), 7.21-7.16 (m, 4H), 5.15 (s, 2H), 4.41 (s, 2H), 3.53 (t, J=6.3 Hz, 2H), 2.98 (s, 3H), 2.91 (t, J=6.3 Hz, 2H), 2.82-2.70 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402680B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-8818a301c88c423e9ac69a81921c7f6e
출처 메모uspto-grants-2008_07