Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl acetate pentane | HCID 22335286 | — |
| Reactant | HCID 59876993 | HCID 59876993 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | HCID 11326643 | HCID 11326643 | 96.3% |
Reaction Steps
To a mixture of 1-methyl-3-(2-chloro-6-fluorophenyl)-5-(3,4-dichloro-5-(2-trimethylsilyl-ethynyl)-thien-2-yl) [1,2,4]triazole (5.0g, 10.9 mmol) in methanol (20 mL) was added potassium carbonate (1.66 g, 12 mmol) at 0° C., and the resulting off-white suspension was stirred at 0° C. for 3.5 hours. TLC analysis (10% EtOAc/Pentane) indicates complete conversion to product. The reaction was acidified with 2 N hydrochloric acid and extracted with ether (2×100 mL). The organics were combined, washed with brine, dried (sodium sulfate), filtered, and the solvent evaporated under reduced pressure to give a tan solid. Trituration with pentane affords 4.06 g (96%) of product as a tan powder: mp 145-165 (slow decomposition) 1H NMR (CDCl3) δ3.77 (s, 1H,), 4.04 (s, 3H), 7.08-7.14 (m, 1H), 7.29-7.40 (Ar-m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06417187B2 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-e486bdc3c84e41f18f61be995ede5a40 |
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| Source note | uspto-grants-2002_07 |
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