HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 2-Furan-2-yl-6-(3-phenoxy-prop-1-ynyl)-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | [1,2,4]Triazolo[1,5-a]pyrazin-8-amine, 6-bromo-2-(2-furanyl)- | HCID 71401630 | — |
| Product | 2-Furan-2-yl-6-(3-phenoxy-prop-1-ynyl)-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine | HCID 11232803 | — |
Reaction Steps
Alternatively, a compound of formula (I) can react with an alkynyl (e.g., a compound of the formula L′-X1a where L′ is a precursor of L and X1a has been defined above) to form an intermediate, which can further react with a compound of the formula R1—X3—Y—X2-L″ to form a compound of formula (I). As an example, 6-bromo-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine can react with prop-2-yn-1-ol to form 3-(8-amino-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazin-6-yl)-prop-2-1-ol, which can then react with phenol in the presence of triphenyl phosphine and diisopropyl azodicarboxylate to form 2-furan-2-yl-6-(3-phenoxy-prop-1-ynyl)-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine, a compound of formula (I). See, e.g., Example 22 below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674791B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-cd222f27e4ed46a599702c3459c014d7 |
| Source note | uspto-grants-2010_03 |