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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453134생성일: 2026년 10월 26일

5-Hydroxyindole → 1H-Indole, 5-[[6-[(phenylmethoxy)methyl]-4-pyrimidinyl]oxy]-

https://huagongshe.com/reaction/453134

반응식

참여 물질

역할이름HCID투입량
반응물5-HydroxyindoleHCID 16054—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물4-((Benzyloxy)methyl)-6-chloropyrimidineHCID 53421259—
용매AcetonitrileHCID 6342—
생성물1H-Indole, 5-[[6-[(phenylmethoxy)methyl]-4-pyrimidinyl]oxy]-HCID 59394260—

반응 단계

To a solution of 5-hydroxy indole (1.33 g, 10 mmol) and 4-benzyloxymethyl-6-chloro-pyrimidine (2.35 g, 10 mmol) in acetonitrile (20 mL) is added DBU. After 16 h at rt the solution is concentrated under reduced pressure. The residue is purified by FCC (EtOAc/Heptane from 0% to 40%) to give 5-(6-benzyloxymethyl-pyrimidin-4-yloxy)-1H-indole. MS (ESI) m/z 447.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492393B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-7cb274b658ab4bdb816a8f488bb21c0a
출처 메모uspto-grants-2013_07