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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1896517생성일: 2026년 10월 26일

methyl 1-chloro-5H-pyrido[4,3-b]indole-4-carboxylate → 1-chloro-5H-pyrido[4,3-b]indole-4-carboxamide

https://huagongshe.com/reaction/1896517

반응식

참여 물질

역할이름HCID투입량
반응물methyl 1-chloro-5H-pyrido[4,3-b]indole-4-carboxylateHCID 59198422—
반응물HCID 178506930HCID 178506930—
용매TetrahydrofuranHCID 8028—
생성물1-chloro-5H-pyrido[4,3-b]indole-4-carboxamideHCID 59198457—

반응 조건

온도100 °C

반응 단계

A mixture containing methyl 1-chloro-5H-pyrido[4,3-b]indole-4-carboxylate and LiNH2 (prepared in situ from ammonia and n-BuLi; 1.0 M in THF; 3.5 equiv) in THF (0.09 M) was heated in a microwave reactor at 100° C. for 1 min in a sealed tube. The reaction mixture was cooled to room temperature and partitioned between EtOAc and saturated NaHCO3. After separation of the organic phase, the aqueous phase was extracted again with EtOAc, and the combined organic phases were washed with brine, dried over MgSO4 and filtered. After evaporation of the organic solvent, the residue was purified by flash chromatography (10-70% EtOAc in hexanes) to provide the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518964B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-3fac0b86374e4f22b38c2e6e188545ea
출처 메모uspto-grants-2013_08