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HRID 549428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/549428

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US07943654B2
出典データセットuspto-grants-2011_05
ORD IDord-7820bae5e1c742a08cb8f7fa518e056d
出典メモuspto-grants-2011_05