Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 53955924 | HCID 53955924 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22993994 | HCID 22993994 | 33% |
Reaction Steps
To a solution of 200 mg (0.412 mmol) of 5-[3-(3-methoxymethoxy-phenyl)-[1,2,4]oxadiazol-5-yl]-N2-(3,4,5-trimethoxy-phenyl)-thiazole-2,4-diamine (prepared in Example B(4)) in 8 mL of 50% aqueous dioxane was added trifluoroacetic acid (8 mL) with water bath cooling at 15° C. After 2 hours at room temperature, toluene was added, and the solution was concentrated in vacuo with the water bath at 22° C. With five milliliters of solvent left, the solution was poured into cold aqueous sodium bicarbonate. This solution was extracted with two portions of dichloromethane, which was subsequently washed with brine and dried over sodium sulfate. Radial silica chromatography eluting with 5-10% methanol/dichloromethane gave 3-{5-[4-amino-2-(3,4,5-trimethoxy-phenylamino)-thiazol-5-yl]-[1,2,4]oxadiazol-3-yl}-phenol (60 mg) as a pale-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620828B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-922804854054402b8c8d1e40c81246d0 |
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| Source note | uspto-grants-2003_09 |
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