Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 59296174 | HCID 59296174 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178432506 | HCID 178432506 | 83.2% |
Reaction Steps
153 mg of 2-Fluoro-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-ylmethoxy]-benzonitrile were dissolved in a mixture of 1 ml tetrahydrofuran and 2 ml methanol. 265 mg hydroxylamine hydrochloride was added followed by the addition of 0.5 ml triethylamine. The reaction mixture was stirred at 60° C. for twenty hours. The solvents were removed in vacuo and the resulting residue poured into water and extracted five times with ethylacetate. The combined organic extracts were washed with brine, dried over MgSO4 and the solvent was evaporated in vacuo to obtain 138 mg of 2-Fluoro-N-hydroxy-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-ylmethoxy]-benzamidine as crude material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709509B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-81af6fb1cae94cf9af2794a1583a44da |
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| Source note | uspto-grants-2010_05 |
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