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HRID 448128作成日:2026年10月26日

Ethyl chloroformate → 5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylate

https://huagongshe.com/reaction/448128

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl chloroformateHCID 10928—
反応物DiisopropylethylamineHCID 81531—
反応物tert-butyl 3-amino-1H-thieno[2,3-c]pyrazole-5-carboxylateHCID 178450636—
溶媒TetrahydrofuranHCID 8028—
生成物5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylateHCID 5773727287.7%

反応手順

A solution of ethyl chlorocarbonate (4.90 mL, 51.7 mmol) in tetrahydrofuran (THF, 60 mL) was slowly added to a mixture of tert-butyl 3-amino-1H-thieno[2,3-c]pyrazole-5-carboxylate (12.0 g, 50.2 mmol) and diisopropylethylamine (DIEA, 51.5 mL, 301 mmol) in THF (300 mL), maintaining the temperature between −5 and −10° C. The reaction was kept at the same temperature for 5 minutes then allowed to reach room temperature. The obtained mixture was evaporated to dryness under vacuum and the residue extracted with ethyl acetate (AcOEt) and water. The organic layer was separated, dried over sodium sulfate and evaporated to dryness. The resulting raw material was triturated with diethyl ether to give 13.7 g of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481584B2
出典データセットuspto-grants-2013_07
ORD IDord-8c28da037f4a46bdac1523c02562e0d1
出典メモuspto-grants-2013_07