HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549514Generated: October 25, 2026
Potassium Carbonate → phenylmethyl 3-(4-amino-6-methyl-1H-indazol-1-yl)benzoate
https://huagongshe.com/reaction/549514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | Benzyl 3-iodobenzoate | HCID 22254461 | — |
| Reactant | HCID 66648350 | HCID 66648350 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | phenylmethyl 3-(4-amino-6-methyl-1H-indazol-1-yl)benzoate | HCID 59010011 | 32.3% |
Reaction Steps
6-Methyl-1H-indazol-4-amine hydrochloride (0.5 g, 2.7 mmol), phenylmethyl 3-iodobenzoate (0.9 g, 2.6 mmol), copper (I) iodide (14 mg, 0.07 mmol), potassium carbonate (1.2 g, 8.68 mmol) and trans-N,N′-dimethyl-1,2-cyclohexanediamine (20 mg, 0.14 mmol) were heated together in DMF (5 mL) at reflux overnight. The mixture was poured into water (15 mL) and ethyl acetate was added to dissolve the resulting oil. The suspension was then filtered through celite. The organic phase was separated, combined with a second ethyl acetate extract, washed successively with water and brine and then dried over anhydrous sodium sulphate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (75 g) eluting with 1 to 5% gradient of ethyl acetate in dichloromethane to give the title compound as a light brown oil (0.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07943651B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-92d902b491c44d9589d6858c8c2895c6 |
|---|
| Source note | uspto-grants-2011_05 |
|---|