Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 10641668 | HCID 10641668 | — |
| Product | HCID 22013874 | HCID 22013874 | 50% |
Reaction Steps
To 3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]propionic acid (1.00 g, 2.85 mmol) obtained in Example 17 was added thionyl chloride (1.7 ml), and the mixture was stirred under heating for 1 hr at 100° C. Excess thionyl chloride was evaporated under reduced pressure and urea (257 mg, 4.28 mmol) was added to the obtained residue. The mixture was stirred under heating for 1 hr at 120° C. and purified by silica gel column chromatography (developing solvent; dichloromethane: methanol=10:1) to give the title compound (560 mg, yield 50%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204277B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-8dc3314deb554596bb582e3215e22397 |
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| Source note | uspto-grants-2001_03 |
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