Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | HCID 68838648 | HCID 68838648 | — |
| Catalyst | Di-n-butyl diacetoxy tin | HCID 9798523 | — |
| Solvent | Tetrahydrofuran toluene | HCID 22635083 | — |
| Product | HCID 68837068 | HCID 68837068 | — |
Reaction Steps
A mixture of the product of Step 1 (0.23 g, 0.787 mmol), ethyl isocyanate (0.28 g, 3.93 mmol) and a catalytic quantity of dibutyltin diacetate (3 drops) in THF/toluene (1:1, 10 mL) was heated in a sealed tube at 100° C. for 15 h. This mixture was cooled to 0° C., the solid obtained was filtered and washed with 10% CHCl3/hexanes to provide the target compound, N-ethyl-N′-[5-(2-methyl-1,3-oxazol-5-yl)-7-pyridin-3-yl[1,2,4]triazolo[1,5-a]pyridin-2-yl]urea as a solid. LCMS (APCI+) 364.
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-6b851651c4054ee4b52dbdd00e6f2f97 |
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| Source note | uspto-grants-2009_04 |
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