Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Malonate → 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Malonate | HCID 7761 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 1,1-Dimethylethyl N-[4-(bromomethyl)-2-pyridinyl]carbamate | HCID 22097736 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester | HCID 54557970 | 62.7% |
반응 단계
To a solution of NaH (80%, 0.17 g, 4.00 mmol) in THF (5 mL) at 0° C. under argon was added diethyl malonate (0.64 g, 4.00 mmol). After the mixture was stirred for 15 min the mixture was added to a refluxed mixture of (4-bromomethyl-pyridin-2-yl)-carbamic acid tert-butyl ester (1.00 g, 3.48 mmol) in THF (10 mL), and the mixture was refluxed for 2 h. The mixture was concentrated under reduced pressure and the residue was partitioned between water and chloroform. The organic layer was washed with water and brine and dried. After filtration and evaporation of the solvent, the crude product was purified by flash chromatography (MeOH/CH2Cl2, 1:100) to give 2-(2-tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester (0.80 g, 55%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07071175B1 |
| 출처 데이터셋 | uspto-grants-2006_07 |
| ORD ID | ord-805b1be0b06a48d0ae30146f8f6f791f |
| 출처 메모 | uspto-grants-2006_07 |