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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1107684생성일: 2026년 10월 25일

Hydrochloric Acid → 3-(1-Methyl-3,5-dichloropyrazol-4-yl)-2-(2-phenylthiazol-4-yl)-3-hydroxyacrylonitrile

https://huagongshe.com/reaction/1107684

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-(2-Phenyl-1,3-thiazol-4-yl)acetonitrileHCID 223844—
반응물3,5-Dichloro-1-methylpyrazole-4-carbonyl chlorideHCID 22169499—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-(1-Methyl-3,5-dichloropyrazol-4-yl)-2-(2-phenylthiazol-4-yl)-3-hydroxyacrylonitrileHCID 5698751563.4%

반응 조건

온도-60 °C

반응 단계

0.72 g of 4-cyanomethyl-2-phenylthiazole was dissolved in 10 ml of dry THF, and 4.6 ml of n-butyl lithium (1.56 M hexane solution) was dropwise added thereto at -60° C. or lower in an argon atmosphere. After the resulting product was stirred at -60° C. or lower for 20 minutes, 0.84 g of 1-methyl-3,5-dichloropyrazole-4-carbonyl chloride as dissolved in 3 ml of dry THF was dropwise added thereto at -60° C. or lower. Then, the resulting product was gradually heated, and stirred for 4 hours at room temperature. The reaction mixture was poured into ice water, acidified with diluted hydrochloric acid, extracted with ethyl acetate, and washed with saturated saline. The resulting product was dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The residual product was purified through silica gel column chromatography to obtain the intended product from the fraction eluted with chloroform. The resulting product was crystallized and washed with diethyl ether to obtain 0.86 g of 3-(1-methyl-3,5-dichloropyrazol-4-yl)-2-(2-phenylthiazol-4-yl)-3-hydroxyacrylonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06063734
출처 데이터셋uspto-grants-2000_05
ORD IDord-87b26d1bda1544068990afc1f4186fc6
출처 메모uspto-grants-2000_05