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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 508613생성일: 2026년 10월 23일

Pinacolone → 5-tert-Butyl-1-(4-methanesulfonyl-phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/508613

반응식

참여 물질

역할이름HCID투입량
반응물PinacoloneHCID 6416—
반응물Diethyl OxalateHCID 7268—
반응물4-(Methylsulphonyl)phenylhydrazineHCID 70142—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물5-tert-Butyl-1-(4-methanesulfonyl-phenyl)-1H-pyrazole-3-carboxylic acid ethyl esterHCID 5964934657%

반응 단계

To a solution of 1M NaHMDS in THF in 120 mL of THF was added dropwise pinacolin (3.1 mL, 25 mmol) at 78° C. After 1 hour, diethyl oxalate (3.7 mL, 27.5 mmol) was added dropwise. The reaction mixture was allowed to warm up to room temperature and stirred overnight. The reaction was quenched by adding 1N HCl solution (50 mL). The reaction mixture was extracted with EtOAc and dried with MgSO4. The mixture was concentrated in vacuo. The product 2h was used without further purification. To a solution of 2h (1 g, 5 mmol) in EtOH (50 mL) was added 4-methylsulfonylphenylhydrazine 1a (1.22 g, 5.5 mmol) at room temperature. The reaction mixture was stirred overnight and refluxed for 3 hour. After cooling, the solvent was removed in vacuo. The resulting solid was purified by column chromatography with hexanes/EtOAc (1:1) to afford the titled compound (1 g, 57% yield) as a white solid. mp 174.9-177.6° C. 1H NMR (300 MHz, DMSO-d6): δ 8.11 (d, J=9 Hz, 2H), 7.80 (d, J=9 Hz, 2H), 6.76 (s, 1H), 4.27 (q, J=7 Hz, 2H), 3.35 (s, 3H), 1.27 (t, J=7 Hz, 3H), 1.16 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096532B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-f6a56d8d4be1467b83ca038eeb0a6c16
출처 메모uspto-grants-2015_08