HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(benzyloxy)-3-oxopropanoate → HCID 178517543, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(benzyloxy)-3-oxopropanoate | HCID 19903223 | — |
| Reactant | 2-Chloropyridine-4-carboximidamide | HCID 50988635 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178517543 | HCID 178517543 | 66% |
Reaction Steps
A mixture of crude ethyl 2-(benzyloxy)-3-oxopropanoate (all from previous step), 2-chloropyridine-4-carboximidamide (9.57 g, 50 mmol) and 100 mL of anhydrous ethanol was refluxed for 4 h under nitrogen. The mixture was then cooled and the volatile solvents were removed by rotary-evaporator. The residue was re-dissolved in water and filtered. The filtrate was acidified by HCl (4N aq) in an ice bath and the white precipitate was filtered, washed with water, and dried to give 5-(benzyloxy)-2-(2-chloropyridin-4-yl)pyrimidin-4-ol (10.4 g, 66%). 1H NMR δ (400 MHz, d6-DMSO): 13.12 (s, 1H), 8.58 (d, J=5.2 Hz, 1H), 8.12 (s, 1H), 8.04 (d, J=5.2 Hz, 1H), 7.94 (s, 1H), 7.51-7.34 (m, 5H), 5.20 (s, 2H); MS (ESI) m/z (M++H)+ 314.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260413B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-c8e27d6be1ba40568755340dbf21efba |
| Source note | uspto-grants-2016_02 |