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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70243생성일: 2026년 10월 24일

Water → methyl N-[[2-chloro-5-[1-[3-(1-methylethyl)-1,2,4-thiadiazol-5-yl]-1H-pyrazol-3-yl]phenyl]methyl]carbamate

https://huagongshe.com/ko/reaction/70243

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물5-Chloro-3-(propan-2-yl)-1,2,4-thiadiazoleHCID 12874683—
반응물HCID 178502067HCID 178502067—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물methyl N-[[2-chloro-5-[1-[3-(1-methylethyl)-1,2,4-thiadiazol-5-yl]-1H-pyrazol-3-yl]phenyl]methyl]carbamateHCID 66790093—

반응 조건

온도165 °C

반응 단계

A mixture of methyl N-[[2-chloro-5-(1H-pyrazol-3-yl)phenyl]methyl]carbamate (i.e. the product of Step B, Example 4) (0.02 g, 0.75 mmol), 5-chloro-3-(1-methylethyl)-1,2,4-thiadiazole (i.e. the product of Step A) (0.61 g, 3.75 mmol) and potassium carbonate (0.25 g, 1.5 mmol) in N-methyl-2-pyrrolidinone (2.5 mL) was heated in a Biotage Creator XM microwave apparatus at 165° C. for 15 minutes. The reaction mixture was poured into water (60 mL), and the aqueous mixture was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with water, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by medium pressure liquid chromatography (0 to 100% gradient of ethyl acetate in hexanes as eluant) to provide the title compound, a compound of the present invention, as a solid (0.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822521B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7efc3d027cd1408baeec34c073293e2a
출처 메모uspto-grants-2014_09