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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 455027생성일: 2026년 10월 25일

Methyl indoline-2-carboxylate → Methyl 1-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)indoline-2-carboxylate

https://huagongshe.com/reaction/455027

반응식

참여 물질

역할이름HCID투입량
반응물Methyl indoline-2-carboxylateHCID 2794655—
반응물3-((1H-imidazol-1-yl)methyl)-6-methyl-2-p-tolylimidazo[1,2-a]pyridineHCID 58337071—
반응물3-(Chloromethyl)-2-(4-chlorophenyl)imidazo[1,2-a]pyridine hydrochlorideHCID 67028719—
생성물Methyl 1-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)indoline-2-carboxylateHCID 67028780—

반응 단계

The title compound was prepared according to Method A and the experimentals described for compound 1 from 3-(chloromethyl)-2-(4-chlorophenyl)imidazo[1,2-a]pyridine hydrochloride and methyl indoline-2-carboxylate. M/e+ 418 for C24H21ClN3O2 (M+H)+; 1H-NMR (400 MHz, CDCl3) δ 8.33 (d, J=6.9 Hz, 1H), 7.69 (d, J=8.4 Hz, 2H), 7.64 (d, J=9.1 Hz, 1H), 7.64 (d, J=8.4 Hz, 2H), 7.25 (t, J=6.9 Hz, 1H), 7.09 (t, J=7.7 Hz, 1H), 7.04 (d, J=6.9 Hz, 1H), 6.83 (t, J=6.6 Hz, 1H), 6.75 (t, J=7.7 Hz, 1H), 6.60 (d, J=7.7 Hz, 1H), 4.90 (d, J=14.7 Hz, 1H), 4.62 (d, J=14.7 Hz, 1H), 3.85 (t, J=8.4 Hz, 1H), 3.26 (m, 1H), 3.23 (s, 3H), 2.96 (dd, J=15.7, 8.0 Hz, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497278B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e8dd510a07064508b962f0079b038718
출처 메모uspto-grants-2013_07