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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1247594생성일: 2026년 10월 25일

Triethylamine → Tert-butyl 3-(4-{[(1-adamantylmethyl)amino]-carbonyl}-5-chloropyridin-2-yl)prop-2-ynyl(ethyl)carbamate

https://huagongshe.com/reaction/1247594

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-butyl N-ethyl-N-(prop-2-yn-1-yl)carbamateHCID 18366151—
반응물N-(1-adamantylmethyl)-5-chloro-2-iodoisonicotinamideHCID 21906675—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매AcetonitrileHCID 6342—
생성물Tert-butyl 3-(4-{[(1-adamantylmethyl)amino]-carbonyl}-5-chloropyridin-2-yl)prop-2-ynyl(ethyl)carbamateHCID 2190672966.5%

반응 단계

The sub-titled compound was prepared from N-(1 adamantylmethyl)-5-chloro-2-iodoisonicotinamide (Example 2(i)) (0.40 g), tert-butyl ethyl(prop-2-ynyl)carbamate (Example 7(i)) (0.34 g), copper (I) iodide (0.004 g), bis-triphenyphosphine palladium dichloride (0.014 g), triethylamine (5 ml) and anhydrous acetonitrile (5 ml) by the method of Example 2(iii). The crude product was purified by chromatography on silica gel eluting with iso-hexane:ethyl acetate (9:1 to 7:3) to afford the sub-titled compound (0.30 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129246B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-6d8ec4b762d2485e9095644448ce1180
출처 메모uspto-grants-2006_10