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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77833생성일: 2026년 10월 24일

Trimethylsilylacetylene → 2,6-Pyridinediamine, 3-[2-(trimethylsilyl)ethynyl]-

https://huagongshe.com/ko/reaction/77833

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilylacetyleneHCID 66111—
반응물3-Iodopyridine-2,6-diamineHCID 476218—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2,6-Pyridinediamine, 3-[2-(trimethylsilyl)ethynyl]-HCID 5925547160%

반응 단계

To a mixture of 3-iodo-pyridin-2,6-diamine (20.0 g, 85.2 mmol) described in Manufacturing Example 13-1-1, trimethylsilyl acetylene (24.2 mL, 170 mmol), copper (I) iodide (3.25 g, 17.0 mmol) N,N-diisopropylethylamine (19.1 g, 148 mmol) and N-methylpyrrolidinone (286 mL) was added tetrakis(triphenylphosphine)palladium (0) (9.81 g, 8.52 mmol) under argon atmosphere, which was stirred for 30 minutes at room temperature. The reaction solution was partitioned into water and ethyl acetate. The ethyl acetate layer was washed with water 4 times and dried over sodium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel chromatography (heptane:ethyl acetate=4:1 then 1:1). The solids obtained by concentrating the eluate under a reduced pressure were washed with heptane containing a small amount of ethyl acetate to obtain the title compound (10.5 g, 60.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8b516c37d4ea4c2baa72aa8bf98345ef
출처 메모uspto-grants-2014_09