Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86631506 | HCID 86631506 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86631507 | HCID 86631507 | 73.6% |
Reaction Steps
Added 3 M aqueous sodium hydroxide (4.41 mL, 13.2 mmol) to a mixture of 1-benzoyl-3-(5-bromo-3-(4-cyanophenoxy)pyridin-2-yl)thiourea (3.00 g, 6.62 mmol) and MeOH (50 mL) and heated to 50° C. for 2 hours. Cooled, partitioned between ethyl acetate and water, washed twice with water, brine, dried, and concentrated. Added ethyl acetate (6 mL), heated to try to afford a solution. Added hexanes (8 mL) slowly, and cooled and triturated for 15 minutes. Filtered, to afford the title compound a (1.70 g, 73.6% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354540B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-558afd29ea42401ca1d3404fe9ac6b26 |
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| Source note | uspto-grants-2013_01 |
|---|