HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → [4-(2-Ethylmorpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl 3-ethoxy-3-iminopropionate hydrochloride | HCID 75345 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Ethylmorpholine | HCID 14933206 | — |
| Product | [4-(2-Ethylmorpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetic acid ethyl ester | HCID 136378675 | — |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
In a microwave tube, 0.45 g of 2-ethylmorpholine is placed in 10 ml of ethanol, 2.11 ml of N,N-diisopropylethylamine and 2.29 g of ethyl 3-ethoxy-3-iminopropanoate hydrochloride. The tube is then microwave-heated at 130° C. for 1 hour and then allowed to return to ambient temperature. The reaction mixture is concentrated under reduced pressure. After purification by silica column chromatography, eluent: 90/05 dichloromethane/methanol, 550 mg of [4-(2-ethylmorpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetic acid ethyl ester are obtained in the form of a beige powder, the characteristics of which are the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133168B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-66c32ae1e2cd4563b92bbcebf93c335a |
| Source note | uspto-grants-2015_09 |