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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2354704생성일: 2026년 10월 25일

Triethylamine → {6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZIN-3-YL}CARBAMIC Acid Butyl Ester

https://huagongshe.com/reaction/2354704

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Butyl chloroformateHCID 61140—
반응물[4-(6-Aminopyridazin-3-yl)piperazin-1-yl](2-trifluoromethylphenyl)methanoneHCID 66849536—
용매DichloromethaneHCID 6344—
생성물{6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZIN-3-YL}CARBAMIC Acid Butyl EsterHCID 6684986574%

반응 단계

To a stirred solution of [4-(6-aminopyridazin-3-yl)piperazin-1-yl](2-trifluoromethyl-phenyl)methanone (100 mg, 0.285 mmol) in dichloromethane (5 mL) was added n-butyl chloroformate (0.285 mmol) in the presence of triethylamine (0.313 mmol) at 0° C. The resulting mixture was stirred at ambient temperature for 24 h and then quenched with water (10 mL). The organic phase was washed with water, saturated NaCl, dried over MgSO4 and then concentrated in vacuo to afford the desired product as a white solid (0.095 g, 74% yield). 1H NMR (500 MHz, CDCl3) δ 8.10, 7.73, 7.63, 7.55, 7.36, 7.04, 4.19, 3.96-4.02, 3.89-3.95, 3.61-3.66, 3.52-3.56, 3.32, 1.64-1.70, 1.38-1.46, 0.95.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07754711B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-6548f7a4f4e14b20bcbee6adaf4f621b
출처 메모uspto-grants-2010_07