Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | HCID 68835562 | HCID 68835562 | — |
| Catalyst | Di-n-butyl diacetoxy tin | HCID 9798523 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68835955 | HCID 68835955 | — |
Reaction Steps
A suspension of the product of Step 1 (160 mg, 0.52 mmol), ethylisocyanate (205 μL, 2.6 mmol), and dibutyltin diacetate (5 drops) in dry toluene (6 mL) was heated at 125° C. in a microwave reactor for 1 h. After being cooled at room temperature the precipitated solid was filtered and washed with chloroform. The crude product was purified by flash chromatography (gradient 0-2% methanol/chloroform) to give 1-ethyl-3-[5-(2-methyl-thiazol-5-yl)-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-urea as a solid. MS m/z 380 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524860B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-7f370f825fe44681b848c16f128365bc |
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| Source note | uspto-grants-2009_04 |
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