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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2389269생성일: 2026년 10월 27일

Triethylamine → Tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2389269

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Tert-butyl 4-(2-carbamoylbenzofuran-5-yl)piperazine-1-carboxylateHCID 11244883—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylateHCID 67154775—

반응 조건

온도0 °C

반응 단계

The tert-butyl 4-[2-(aminocarbonyl)-1-benzofuran-5-yl]piperazine-1-carboxylate (85 mg, 0.246 mmol) was dissolved in 5 mL of DCM and cooled to 0° C. under nitrogen. Triethylamine (0.075 mL, 0.541 mmol) was added, followed by trifluoroacetic anhydride (0.038 mL, 0.271 mmol). The reaction was stirred for 1 hour, then was diluted with additional 20 mL of DCM and washed with water (2×40 mL). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to afford tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273737B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-e1c2fb2a86d248208d1585cf22ab9967
출처 메모uspto-grants-2012_09