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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64459생성일: 2026년 10월 23일

Cyclopentanemethanol → N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-(cyclopentylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/ko/reaction/64459

반응식

참여 물질

역할이름HCID투입량
반응물CyclopentanemethanolHCID 77195—
반응물CyanomethylenetributylphosphoraneHCID 4622928—
반응물N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxamideHCID 86713409—
용매TolueneHCID 1140—
생성물N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-(cyclopentylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamideHCID 86713474—

반응 조건

온도110 °C

반응 단계

A mixture of 120 mg of N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxamide, 60 μl of cyclopentylmethanol, 156 μl of (tributylphosphoranylidene)acetonitrile, and 2.4 ml of toluene was stirred at 110° C. for 16 hours, followed by purification using silica gel chromatography, to obtain 100 mg of N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-(cyclopentylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447090B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-5ab65197b73f4c0aac187c473560d72d
출처 메모uspto-grants-2016_09