HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,1-Dimethylethyl N-[4-(bromomethyl)-2-pyridinyl]carbamate | HCID 22097736 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester | HCID 54557970 | 62.7% |
Reaction Steps
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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071175B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-805b1be0b06a48d0ae30146f8f6f791f |
| Source note | uspto-grants-2006_07 |