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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2065020생성일: 2026년 10월 26일

Bromide ion → 4-(4-Nitro-pyrazol-1-ylmethyl)-thiazole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2065020

반응식

참여 물질

역할이름HCID투입량
반응물Bromide ionHCID 259—
반응물NitrogenHCID 947—
반응물Potassium CarbonateHCID 11430—
반응물4-nitro-1H-pyrazoleHCID 16376—
반응물Ethyl 4-(chloromethyl)-1,3-thiazole-2-carboxylateHCID 10822129—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물4-(4-Nitro-pyrazol-1-ylmethyl)-thiazole-2-carboxylic acid ethyl esterHCID 66928895—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-chloromethyl-thiazole-2-carboxylic acid ethyl ester (1.84 g, 8.93 mmol) in acetone (20.0 mL) was treated, under inert atmosphere (N2) with K2CO3 (6.23 g, 44.66 mmol) followed by 4-nitro-1H-pyrazole (1.00 g, 8.93 mmol) and TBA bromide (576 mg, 1.79 mmol). The resulting mixture was stirred at rt overnight. Water (40 mL), followed by EA (50 mL) were added. The aq. layer was extracted with EA (50 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 (50:50 hept-EA) gave the title compound as a yellow oil. TLC: rf (50:50 hept-EA)=0.30. LC-MS-conditions 02: tR=0.90 min; [M+H]+=283.25.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08288419B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-385828603fc9419ea257798b5641aaa9
출처 메모uspto-grants-2012_10