HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 54394959, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl ethyl methylpropanedioate | HCID 13198666 | — |
| Reactant | tert-Butyl (5-(bromomethyl)pyridin-2-yl)carbamate | HCID 23030321 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | HCID 54394959 | HCID 54394959 | 61.5% |
Reaction Steps
A solution of tert-butyl ethyl methylmalonate (457 mg, 2.26 mmol) in DMF (4 mL) was added dropwise to a suspension of NaH (90 mg, 2.26 mmol, 60% in oil) in DMF (4 mL). The reaction mixture was stirred for 20 min. A solution of (5-bromomethyl-pyridin-2-yl)-carbamic acid tert-butyl ester (500 mg, 1.74 mmol) in DMF (2.5 mL) was added and the reaction was stirred for 70 min. EtOAc was added and the mixture was washed with water and brine, dried and concentrated under reduced pressure. Chromathography (Heptane/EtOAc, 3:1→1:3) gave 2-(6-tert-butoxycarbonylamino-pyridin-3-ylmethyl)-2-methyl-malonic acid tert-butyl ester ethyl ester (437 mg, 61% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071175B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-f8a92e98d3404dbf8bf128e5eee8b1de |
| Source note | uspto-grants-2006_07 |