HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyldiazomethane → methyl 1H-indazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 1H-indazole-4-carboxylic acid | HCID 21982323 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl 1H-indazole-4-carboxylate | HCID 6623327 | — |
Reaction Steps
Indazole-4-carboxylic acid (2.00 g, 12.3 mmol) is suspended in methanol (20 mL) and toluene (30 mL) at room temperature. A solution of 2M trimethylsilyl diazomethane (12 mL, 24 mmol) in toluene is added slowly and the mixture is stirred at room temperature until the solution turned yellow. The reaction is quenched with concentrated acetic acid (5 mL) and the solvent is removed in vacuo. The residue is purified by silica gel chromatography eluting with a gradient of 0-30% ethyl acetate in hexanes to afford 1H-indazole-4-carboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056858B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-efcd8f5ef1d6441ea583842ef338f8dc |
| Source note | uspto-grants-2015_06 |