HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Methyl 5-(trifluoromethyl)-1H-indazole-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Methyl 2-amino-3-methyl-5-(trifluoromethyl)benzoate | HCID 118251663 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 5-(trifluoromethyl)-1H-indazole-7-carboxylate | HCID 118251578 | — |
Reaction Steps
To a solution of compound 3, at 0° C. and under nitrogen atmosphere, in chloroform (0.3M) was added acetic anhydride (2.3 equiv.) drop wise and the resulting mixture was stirred for 1 h at r.t. Then potassium acetate (0.2 equiv.) was added followed by addition of isoamyl nitrite (2.2 equiv.) and the resulting mixture was heated at reflux for 16 h. After, the reaction was cooled down to r.t. While cooling, a solid precipitation was observed. The solid was filtrated and dried under vacuum to give the title compound 4. (0.324 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365569B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-d6c86550ca0542cba895e693e06802bb |
| Source note | uspto-grants-2016_06 |