HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595702Generated: October 29, 2026
Hydrochloric Acid → 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carboxylic acid
https://huagongshe.com/reaction/595702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carbonitrile | HCID 90332439 | — |
| Product | 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carboxylic acid | HCID 90332516 | 85% |
Reaction Steps
A suspension of 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carbonitrile (50 mg, 0.14 mmol) in 10% NaOH (5 mL) was heated at 100° C. for 48 h. The reaction mixture was cooled to RT and poured into water (10 mL). After pH was adjusted to 4 with 1 N HCl, the mixture was extracted with EtOAc. The combined organic phases were washed with brine, dried over Na2SO4, filtered and evaporated to get 6-amino-5-bromo-2-(4-fluorophenyl)-2H-indazole-3-carboxylic acid (45 mg, yield: 85%). 1H-NMR (DMSO-d6, 400 MHz) δ 8.20 (s, 1H), 7.77˜7.82 (m, 2H), 7.45˜7.52 (m, 2H), 7.03 (s, 1H), 6.61 (s, 1H), 5.60 (s, 2H). MS (M+H)+: 350/352.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09243002B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-b049edf44a5a4d9b87609a60b4a7a962 |
|---|
| Source note | uspto-grants-2016_01 |
|---|