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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1044779생성일: 2026년 10월 24일

Nitrogen → HCID 86664759, 화합물

https://huagongshe.com/ko/reaction/1044779

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Sodium AzideHCID 33557—
반응물1-(4-Chloromethyl-thiazol-2-yl)ethanoneHCID 66819977—
용매DimethylformamideHCID 6228—
생성물HCID 86664759HCID 86664759—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 1-(4-chloromethyl-thiazol-2-yl)-ethanone (1.08 g, 6.13 mmol) in dry DMF (21 mL) and treated with NaN3 (1.20 g, 18.39 mmol) at 65° C. until completion of the reaction. The reaction mixture was then cooled down to rt and partitioned between EA and water. The layers were separated and the org. layer dried over MgSO4, filtered and concentrated under reduced pressure to give crude 1-(4-(azidomethyl)-thiazol-2-yl)-ethanone as a yellow oil. To a solution of the crude azide (200 mg, 1.10 mmol) in THF (6 mL) were added polymer-supported Ph3P (2.0 eq.) and water (2 mL). The reaction mixture was stirred at 60° C. until completion of the reaction, cooled down to rt and filtered. The filtrate was partitioned between EA and aq. sat. NaHCO3 and the layers separated. The org. layer was dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a brown oil after purification by FC (CH2Cl2-MeOH-Et3N). LC-MS-conditions 01: tR=0.26 min; [M+H]+=157.04.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08563714B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-f36e7442c31e4460b6918ebd8b5fd132
출처 메모uspto-grants-2013_10