HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → HCID 178517896, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-(benzyloxy)acetate | HCID 290299 | — |
| Reactant | Sulfuric acid--morpholine-4-carboximidamide (1/1) | HCID 12427953 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178517896 | HCID 178517896 | — |
Reaction Steps
The 4-alkoxy-2-morpholino-5-pyrimidinols (D represents alkoxy) can be prepared by reacting a 1:1 mixture of ethyl benzyloxyacetate and ethyl formate with sodium hydride in toluene and the product is then reacted with 4-morpholinecarboximidamide sulfate to give 5-benzyloxy-2-morpholino-4-pyrimidinol. The latter compound is converted to 5-benzyloxy-4-chloro-2-morpholinopyrimidine by reaction with phosphorus oxychloride. The ring chlorine is then replaced by an alkoxy group with an alkali alkoxide to give 4-alkoxy-5-benzyloxy-2-morpholinopyrimidine. The benzyloxy group is then converted to the OH group by hydrogenation in the presence of a solvent and a hydrogenation catalyst.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892732 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-62ae6666699b4bb79835ca1c0763c163 |
| Source note | uspto-grants-1990_01 |