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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2065053생성일: 2026년 10월 26일

Bromide ion → 2-(2-Methyl-[1,3]dioxolan-2-yl)-5-(4-nitro-pyrazol-1-ylmethyl)-thiazole

https://huagongshe.com/reaction/2065053

반응식

참여 물질

역할이름HCID투입량
반응물Bromide ionHCID 259—
반응물NitrogenHCID 947—
반응물Potassium CarbonateHCID 11430—
반응물4-nitro-1H-pyrazoleHCID 16376—
반응물5-Chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 66928793—
용매AcetoneHCID 180—
생성물2-(2-Methyl-[1,3]dioxolan-2-yl)-5-(4-nitro-pyrazol-1-ylmethyl)-thiazoleHCID 66928734—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 5-chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazole (495 mg, 2.25 mmol) in acetone (1.0 mL) was added to a solution of 4-nitro-1H-pyrazole (268 mg, 2.37 mmol) in acetone (1.0 mL). K2CO3 (1.57 g, 11.27 mmol) followed by TBA bromide (145 mg, 0.45 mmol) were added and the reaction mixture was stirred at rt until completion. The solvent was removed under reduced pressure and water (10 mL) followed by EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (10:1 to 2:1 hept-EA) gave the title compound as a yellow oil. TLC: rf (1:2 hept-EA)=0.24. LC-MS-conditions 01: tR=0.82 min, [M+H]+=296.93.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08288419B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-4c19350b35c8489dbebb8f711c6e2315
출처 메모uspto-grants-2012_10