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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448128생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/448128

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물DiisopropylethylamineHCID 81531—
반응물tert-butyl 3-amino-1H-thieno[2,3-c]pyrazole-5-carboxylateHCID 178450636—
용매TetrahydrofuranHCID 8028—
생성물5-tert-butyl 1-ethyl 3-amino-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylateHCID 5773727287.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481584B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-8c28da037f4a46bdac1523c02562e0d1
출처 메모uspto-grants-2013_07