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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2404491생성일: 2026년 10월 26일

2'-Hydroxybenzophenone → 2-[(6-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]-4-fluorophenyl]hex-5-ynylimino)phenylmethyl}phenol

https://huagongshe.com/reaction/2404491

반응식

참여 물질

역할이름HCID투입량
반응물2'-HydroxybenzophenoneHCID 8348—
반응물OxalateHCID 71081—
반응물6-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]-4-fluorophenyl}hex-5-ynylamineHCID 66836161—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물2-[(6-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]-4-fluorophenyl]hex-5-ynylimino)phenylmethyl}phenolHCID 136335847—

반응 단계

A mixture of 6-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]-4-fluorophenyl}hex-5-ynylamine, oxalate (example 557, 70 mg), 2-hydroxybenzophenone (30 mg) in ethanol (4 mL) is refluxed for 4 h. The mixture is then cooled, diluted with water and extracted with ethyl acetate. Pooled extracts are dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography over silica gel (gradient dichloromethane/methanol/ammonia from 100/0/0 to 90/10/0.5) to afford 2-[(6-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]-4-fluorophenyl]hex-5-ynylimino)phenylmethyl}phenol. TLC (Eluent: CH2Cl2/MeOH/NH4OH 95/5/0.5) Rf=0.15.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08802664B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-ae4e6df297de42c5b9dd351ac59ff374
출처 메모uspto-grants-2014_08