HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054806Generated: November 4, 2026
Potassium Carbonate → 6-Chloro-5-(4-isopropoxyphenyl)-1H-indazole-3-carboxylic acid
https://huagongshe.com/reaction/1054806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Isopropoxybenzeneboronic acid | HCID 3698726 | — |
| Reactant | 5-bromo-6-chloro-1H-indazole-3-carboxylic acid | HCID 86698791 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Chloro-5-(4-isopropoxyphenyl)-1H-indazole-3-carboxylic acid | HCID 86698798 | 11% |
Reaction Steps
A mixture of 5-bromo-6-chloro-1H-indazole-3-carboxylic acid (100 mg, 0.36 mmol), 4-isopropoxyphenylboronic acid (68.6 mg, 0.38 mmol), and 2 N aqueous potassium carbonate solution (1.1 mL, 2.2 mmol) in toluene (1.6 mL) and EtOH (2.4 mL) was degassed with N2 and treated with [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane adduct (29.4 mg, 0.036 mmol) under N2. The reaction mixture was sealed in a pressure tube and heated to 110° C. for 1 hour. The cooled reaction mixture was acidified to pH 5 and concentrated in vacuo. The resulting solid was purified by reverse phase HPLC (Column: Waters XBridge C18 19×100 mm, 5 μm; Mobile phase A: 0.03% NH4OH in water (v/v); Mobile phase B: 0.03% NH4OH in MeCN (v/v); 95.0% H2O/5.0% MeCN linear to 50.0% H2O/50.0% MeCN in 10.5 min, 50.0% H2O/50.0% MeCN linear to 0% H2O/100% MeCN in 0.5 min HOLD at 0% H2O/100% MeCN from 11.0 to 12.0 min. Flow: 25 mL/min) to give the title compound (13.0 mg, 11% yield). MS (ES+) 331.1 (M+H)+. Retention time=3.05 minutes (Column: Waters Atlantis dC18 4.6×50 mm, 5 μm; Mobile phase A: 0.05% TFA in water (v/v); Mobile phase B: 0.05% TFA in MeCN (v/v); Gradient: 95:5 A:B linear to 5:95 A:B in 4.0 min, hold at 5:95 A:B to 5.0 min. Flow: 2 mL/min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09394285B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-14296b46093b41bd868b1d1077372c16 |
|---|
| Source note | uspto-grants-2016_07 |
|---|