HuagongsheHuagongshe Chemistry Print Report · For research reference only
Uracil → HCID 10670845, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Uracil | HCID 1174 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | beta-D-Glucose pentaacetate | HCID 2724702 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 10670845 | HCID 10670845 | — |
Reaction Steps
Uracil is bis-trimethylsilylated according to the procedure of Niedballa and Vorbruggeno Uracil is dissolved in benzene, and added to 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranose 33.1b (Xi=β-OAc) (Niedbala and Vorbruggen) in 1,2 dichloroethane followed by tin tetrachloride in 1,2-dichloroethane according to the method of Vorbruggen and Niedballa to provide the 1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)uracil 33.1b (Xi=β-uracil-1-yl). Following methanolysis with sodium methoxide in methanol the 1-(B-D-glucopyranosyl)uracil 33.1a (Xi=β-uracil-1-yl) is obtained. This is converted into the morpholino subunit 32.2b (Xi=β-uracil-1-yl) by the general procedure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05506337 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-46645776da004e07b2b86cde78eb70b5 |
| Source note | uspto-grants-1996_04 |