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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230066생성일: 2026년 10월 25일

Triethylamine → 2-(Methoxycarbonyl)-5-nitrophenyl 4-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/230066

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-MethylpiperazineHCID 53167—
반응물DiisopropylethylamineHCID 81531—
반응물TriphosgeneHCID 94429—
반응물Salicylic acid, 4-nitro-, methyl esterHCID 139539—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물2-(Methoxycarbonyl)-5-nitrophenyl 4-methylpiperazine-1-carboxylateHCID 57632925—

반응 조건

온도0 °C

반응 단계

To a dry flask are added 2-hydroxy-4-nitro-benzoic acid methyl ester (40 mmol) (from Example 1h) and triphosgene (26.6 mmol) and DCM (100 mL). The reaction mixture is cooled to 0° C. and diisopropylethylamine (40 mmol) is added slowly. After addition the mixture is warmed to rt. After 1 h at this temperature it is refluxed for 1 h. The mixture is cooled down and the solvents are removed. THF (100 mL), Et3N (80 mmol), and N-methyl piperazine (80 mmol) are added and the mixture is stirred at rt overnight. The solvent is removed and the residue dissolved in EtOAc. Phases are separated upon addition of a 10% solution of NaHCO3. The organic phase is washed with brine, dried on Na2SO4 and evaporated. The crude is used in the following reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07563894B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-ff89afc63ad34974acc5de0ac8fb91c3
출처 메모uspto-grants-2009_07