Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 2110925 | HCID 2110925 | — |
| Reactant | HCID 178418800 | HCID 178418800 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19860555 | HCID 19860555 | — |
Reaction Steps
To a solution of 82 mg of 4-methylimidazole in 10 ml of tetrahydrofuran at 5° C. was added 50 mg of sodium hydride in 50% oil and the resulting mixture stirred at 5° C. for 20 minutes. 2-(o-Methoxyphenyl)-4-chloromethylthiazole (240 mg) in 5 ml of the same solvent was added and the reation mixture heated at reflux for 2 hours. The reaction mixture was cooled to room temperature and treated with 1 ml of water. The water and solvent were removed in vacuo and the residue dissolved in chloroform. The chloroform solution was washed with a brine solution, dried over sodium sulfate and concentrated to give 250 mg of crude product. The product was obtained by chromatography on 7 g of silica gel (chloroform-methanol), 40:1-v:v), 100 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04914207 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-ba226cb262d54e6da36641c9459faac8 |
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| Source note | uspto-grants-1990_04 |
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