HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 1,3-diethyl-1H-indazole-6-carboxylic acid methoxy-methyl-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178438012 | HCID 178438012 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-diethyl-1H-indazole-6-carboxylic acid methoxy-methyl-amide | HCID 59810833 | 111.2% |
Reaction Steps
A mixture of potassium tert-butoxide (0.144 g, 1.28 mmol) and iodoethane (0.20 g, 1.28 mmol) in THF (1 mL) was added to a solution of 3-ethyl-1H-indazole-6-carboxylic acid methoxy-methyl-amide (0.20 g, 0.86 mmol) in THF (3 mL) and the resulting mixture stirred at room temperature for 16 hours. Ethyl acetate (30 mL) was then added and the product was extracted with 0.5 N HCl (10 mL). The aqueous layer was then re-extracted with ethyl acetate (30 mL). The organics were combined, dried, filtered and concentrated to afford 250 mg of 1,3-diethyl-1H-indazole-6-carboxylic acid methoxy-methyl-amide that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432266B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-5fbfcbd2e161455e8c12ef604d297d23 |
| Source note | uspto-grants-2008_10 |