참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diphosgene | HCID 10426 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzyl piperazine-1-carboxylate | HCID 643495 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Cbz-piperazine-1-carbonyl Chloride | HCID 19358568 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08658794B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-93d41685d4594b559bf4b545dc029326 |
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| 출처 메모 | uspto-grants-2014_02 |
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