Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | HCID 10357392 | HCID 10357392 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10474323 | HCID 10474323 | 82% |
Reaction Steps
To a solution of [2-(3-Isopropyl-[1,2,4]triazolo[4,3-a]pyridin-6-ylsulfanyl)-phenyl]-methanol (45.0 mg, 0.15 mmol) in dichloromethane (1.5 mL) under nitrogen at ambient temperature was added ethyl isocyanate (12.0 μL, 0.15 mmol). The reaction was heated to 50° C. for 1 hour. The reaction was cooled, ethyl isocyanate added (30 μL, 0.38 mmol), and stirred at ambient temperature for 16 hours. The reaction was concentrated in vacuo to an oil. The residue was triturated from ether to give the title compound (45 mg, 82%). MS (M+1)=371.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07321040B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-d0acbbc07fe5481f88b98e0e8774ce94 |
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| Source note | uspto-grants-2008_01 |
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