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HRID 1496649作成日:2026年10月27日

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/reaction/1496649

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物5-Chloro-3-(propan-2-yl)-1,2,4-thiadiazoleHCID 12874683—
反応物HCID 178502067HCID 178502067—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物methyl N-[[2-chloro-5-[1-[3-(1-methylethyl)-1,2,4-thiadiazol-5-yl]-1H-pyrazol-3-yl]phenyl]methyl]carbamateHCID 66790093—

反応条件

温度165 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09198433B2
出典データセットuspto-grants-2015_12
ORD IDord-608a571d25ee44bcb4ed761127bee3a2
出典メモuspto-grants-2015_12