Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-[4-(Methylsulfanyl)phenyl]urea | HCID 306638 | — |
| Reactant | HCID 19391054 | HCID 19391054 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15295073 | HCID 15295073 | 39.2% |
Reaction Steps
Acetic acid (1.08 g; 18 mmol), 4.5 g (24.7 mmol) of the compound of Example 5 and 5.0 g (18 mmol) of the compound of Example 1 were dissolved in 180 ml of toluene. The resulting solution was heated to reflux, stirred at that temperature for 4 hours and then cooled to room temperature. The cooled solution was washed with a IN hydrochloric acid solution, a saturated sodium bicarbonate solution, water and a saturated brine solution. The washed solution was then filtered to remove any solid particulates which had formed and the liltrate was concentrated to dryness to provide a residue. This residue was purified by column chromatography using a 20-40% ethyl acetate in hexane gradient as eluent. Fractions containing the above titled compound were combined and then concentrated to dryness to provide 3.14 g of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05441984 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-fb923c617bfe4b63a8c577f4cb4c064d |
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| Source note | uspto-grants-1995_08 |
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