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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245701생성일: 2026년 10월 25일

Diphosgene → 4-Cbz-piperazine-1-carbonyl Chloride

https://huagongshe.com/reaction/245701

반응식

참여 물질

역할이름HCID투입량
반응물DiphosgeneHCID 10426—
반응물DiisopropylethylamineHCID 81531—
반응물Benzyl piperazine-1-carboxylateHCID 643495—
용매TetrahydrofuranHCID 8028—
생성물4-Cbz-piperazine-1-carbonyl ChlorideHCID 19358568—

반응 조건

온도0 °C

반응 단계

Trichloromethyl chloroformate (5.45 mmol, 0.657 ml) in tetrahydrofuran (20 ml) was cooled to 0° C. and a solution of benzyl 1-piperazinecarboxylate (4.54 mmol, 0.876 ml) and N,N-diisopropylethylamine (9.99 mmol, 1.651 ml) in tetrahydrofuran (20 ml) was added dropwise. After stirring for one hour at 0° C. the solids were removed by filtration over decalite and the filtrate was concentrated in vacuo to give crude benzyl 4-(chlorocarbonyl)piperazine-1-carboxylate. The latter compound was added to 2-aminomethyl-3-chloropyrazine hydrochloride (content 69%; 3.49 mmol, 0.91 g) in dichloromethane (15 ml) and triethylamine (10.46 mmol, 1.458 ml) and the reaction mixture was stirred over night at room temperature. Then the reaction mixture was filtered over decalite (washed with dichloromethane). The filtrate was concentrated and the crude product was purified using column chromatography (silica gel; dichloromethane with gradient 0 to 10% methanol) to give benzyl 4-((3-chloropyrazin-2-yl)methylcarbamoyl)piperazine-1-carboxylate (1.15 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658794B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-93d41685d4594b559bf4b545dc029326
출처 메모uspto-grants-2014_02