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HRID 615809作成日:2026年10月26日

Pyrazole → Methyl (5-tert-butyl-1H-pyrazol-3-yl)carbamate

https://huagongshe.com/reaction/615809

反応式

関与物質

役割名称HCID仕込み量
反応物PyrazoleHCID 1048—
反応物Methyl chloroformateHCID 6586—
反応物Potassium CarbonateHCID 11430—
反応物3-Amino-5-tert-butylpyrazoleHCID 522787—
溶媒Carbon TetrachlorideHCID 5943—
生成物Methyl (5-tert-butyl-1H-pyrazol-3-yl)carbamateHCID 1346950126.8%

反応手順

10 g of 3-amino-5-t-butylpyrazole as prepared in Reference Example (this pyrazole compound being hereinafter referred to as "Compound [II]") was dissolved in 100 ml of carbon tetrachloride, and 6.8 g of methyl chloroformate was added to the solution. The mixture was then allowed to react for 5 hours under refluxing. After cooling the reaction solution, a potassium carbonate aqueous solution was added thereto whereby crystals were formed. The crystals were collected by filtration, and washed with carbon tetrachloride and water to obtain 3.8 g of methyl N-(5-t-butyl-3-pyrazolyl)carbamate. This compound was recrystallized from a mixed solvent of carbon tetrachloride and chloroform and found to have a melting point of 177° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04501606
出典データセットuspto-grants-1985_02
ORD IDord-e91c6fe96a9642a5a48384cf49a8d376
出典メモuspto-grants-1985_02