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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60211생성일: 2026년 10월 23일

Propyne → HCID 58365135, 화합물

https://huagongshe.com/ko/reaction/60211

반응식

참여 물질

역할이름HCID투입량
반응물PropyneHCID 6335—
반응물TriethylamineHCID 8471—
반응물2-Amino-5-bromo-3-iodopyridineHCID 1516508—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TetrahydrofuranHCID 8028—
생성물HCID 58365135HCID 58365135—

반응 조건

온도-40 °C

반응 단계

Propyne (28 g, 700 mmol) was condensed into a pre-weighed flask cooled to ca. −40° C. containing THF (150 mL). The solution was added via cannula to a cooled (0-5° C.), degassed mixture of 5-bromo-3-iodo-pyridin-2-ylamine (139 g, 465 mmol), bis(triphenylphosphine)dichloropalladium(0) (16.3 g, 23.2 mmol), copper (I) iodide (5.3 g, 27.9 mmol) and triethylamine (141 g, 194 mL, 1.4 mol) in THF (1.25 L). The mixture was stirred at 0-5° C. for 30 minutes then for a further 30 minutes at ambient temperature. The solid was removed by filtration and the cake washed with THF. The filtrate was diluted with ethyl acetate and extracted with 2M hydrochloric acid (×3). The combined acid extract was washed with diethyl ether and then made basic by careful addition of potassium carbonate then extracted with diethyl ether (×3). The combined organic layer was dried (Na2SO4), filtered and evaporated to afford the title compound as a buff solid (91 g, 93%). 1H NMR (400 MHz, CDCl3): 8.01 (d, J=2.4 Hz, 1H), 7.55 (d, J=2.4 Hz, 1H), 4.96 (s, 2H), 2.11 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440976B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-66a9948b13f44e0cb59fdfb3122dd571
출처 메모uspto-grants-2016_09