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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1691326생성일: 2026년 10월 27일

Triethylamine → 3-(3-(4-Benzyloxy-benzyl)-isoxazol-5-yl)-pyridine

https://huagongshe.com/reaction/1691326

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-EthynylpyridineHCID 186003—
반응물4-Benzyloxy-phenyl-acetohydroximoyl chlorideHCID 72262873—
용매TetrahydrofuranHCID 8028—
생성물3-(3-(4-Benzyloxy-benzyl)-isoxazol-5-yl)-pyridineHCID 4985018248.2%

반응 단계

To a tetrahydrofuran (3 mL) solution of 3-ethynylpyridine (50 mg, 0.485 mmol) and (4-benzyloxy-phenyl)-acetohydroximoyl chloride (214 mg, 0.776 mmol) described in Manufacturing Example 1-1-3 was added triethylamine (270 μL, 1.94 mmol), which was stirred for 2.5 hours at room temperature. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:4 to 1:2) to obtain the title compound (80 mg, 48%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153662B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-b77440e307e34c68a0facaec1a664dc8
출처 메모uspto-grants-2012_04