Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiazole | HCID 9256 | — |
| Reactant | HCID 131713133 | HCID 131713133 | — |
| Product | HCID 13457515 | HCID 13457515 | — |
Reaction Steps
A mixture of 2.0 g of the phosphate ester obtained in Example 10 and 4.5 g of thiazole is stirred and warmed at 60° C. for 5 days. The thiazole is distilled off under reduced pressure, and 50 ml of methanol and 2 g of silver carbonate are added to the residue. The mixture is heated under reflux for 2 hours. After filtration, the filtrate is evaporated to dryness, and the residue is separated and purified by silica gel chromatography [eluent: chloroform-methanol-water (65:25:4)] and crystallized from chloroform-acetone to obtain the contemplated product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04408052 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-8566530c7fe14012aa39defbab456bc9 |
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| Source note | uspto-grants-1983_10 |
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