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HRID 253405생성일: 2026년 10월 25일

1H-Pyrrolo(2,3-b)pyridine → 3-[3-(4-chloro-benzyloxy)-2-ethoxy-benzyl]1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/253405

반응식

참여 물질

역할이름HCID투입량
반응물1H-Pyrrolo(2,3-b)pyridineHCID 9222—
반응물1,1,1-Trifluoro-2-iodoethaneHCID 67709—
반응물Ethane, 1-fluoro-2-iodo-HCID 69804—
반응물4-Chloro-2-fluorobenzyl bromideHCID 2736551—
반응물Oxazole, 4,5-dihydro-4-ethyl-2-((4-methoxyphenyl)methyl)-, (+-)-HCID 3041214—
반응물5-methoxy-1H-pyrrolo[2,3-b]pyridineHCID 10307871—
생성물3-[3-(4-chloro-benzyloxy)-2-ethoxy-benzyl]1H-pyrrolo[2,3-b]pyridineHCID 58087711—

반응 단계

were prepared following the protocol of Scheme 20, substituting iodoethane with iodomethane in Step 3 to provide P-1891, or substituting iodoethane with 2-iodo-1,1,1-trifluoroethane in Step 3 to provide P-2076, or substituting iodoethane with 2-iodo-1-fluoroethane in Step 3 to provide P-2118, or substituting 4-chlorobenzyl bromide 22 with 4-chloro-2-fluoro-benzyl bromide in Step 1 and 7-azaindole 6 with 5-methoxy-7-azaindole in Step 4 to provide P-2016. MS (ESI) [M+H+]+=393.4 (P-1891), 461.08 (P-2076), 455.2 (P-2016), and 425.17 (P-2118).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872018B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-21908bb60a934dd9b9317683fa3c0932
출처 메모uspto-grants-2011_01