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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247591생성일: 2026년 10월 25일

tert-butyl N-(prop-2-yn-1-yl)carbamate → tert-Butyl 3-(4-{[(1-adamantylmethyl)amino]carbonyl}-5-chloropyridin-2-yl)prop-2-ynylcarbamate

https://huagongshe.com/reaction/1247591

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
반응물N-(1-adamantylmethyl)-5-chloro-2-iodoisonicotinamideHCID 21906675—
용매AcetonitrileHCID 6342—
용매TriethylamineHCID 8471—
생성물tert-Butyl 3-(4-{[(1-adamantylmethyl)amino]carbonyl}-5-chloropyridin-2-yl)prop-2-ynylcarbamateHCID 2190667474.4%

반응 단계

A suspension of N-(1-adamantylmethyl)-5-chloro-2-iodoisonicotinamide (Example2(i)) (0.43 g) and tert-butyl prop-2-ynylcarbamate, (0.31 g) in anhydrous acetonitrile (5 ml) and triethylamine (5 ml) was purged with nitrogen for 5 minutes and the copper (I) iodide (0.004 g) and bis-triphenyphosphine palladium dichloride (0.014 g) were added. The mixture was stirred under nitrogen for 0.75 hours. The mixture was concentrated and the residue was purified by chromatography on silica gel eluting with acetone:dichloromethane (1:19) to afford the sub-titled compound (0.34 g) as a yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129246B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-8bab744f2d184a70b0f0f08a29c1889c
출처 메모uspto-grants-2006_10