참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-Methylpiperazine | HCID 53167 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Triphosgene | HCID 94429 | — |
| 반응물 | Salicylic acid, 4-nitro-, methyl ester | HCID 139539 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(Methoxycarbonyl)-5-nitrophenyl 4-methylpiperazine-1-carboxylate | HCID 57632925 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07563894B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-ff89afc63ad34974acc5de0ac8fb91c3 |
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| 출처 메모 | uspto-grants-2009_07 |
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