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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862170Generated: November 2, 2026

4-Aminophenol → HCID 178520042, compound

https://huagongshe.com/reaction/1862170

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 178520043HCID 178520043—
SolventDimethylformamideHCID 6228—
ProductHCID 178520042HCID 178520042—

Reaction Steps

To a solution of 3-formyl-1H-indazole-6-carboxylic acid (1.6 g, 8.4 mmol) and 4-aminophenol (1.8 g, 16.8 mmol) in dry dimethylformamide (35 mL) was added HATU (3.8 g, 16.8 mmol) followed by triethylamine (1.4 mL, 10.1 mmol). The reaction was stirred at room and monitored by TLC and LC/MS. After two hours the reaction was complete. The solvent was removed by vacuum and the product was purified by flash column chromatography using ethyl acetate: petroleum ether 1:1 to pure ethyl acetate. N-(4-Hydroxyphenyl)-3-formyl-1H-indazole-6-carboxamide was isolated as a tan colored solid. 1H NMR (DMSO-d6) δ 6.79 (2H, d, 8.9 Hz), 7.59 (2H, d, 8.9 Hz), 7.94 (1H, d, 9.8 Hz), 8.24 (1H, d, 8.2 Hz), 8.31 (1H, s), 9.31 (1H, br s), 10.27 (2H, s) (APCI pos) 282.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534524B1
Source datasetuspto-grants-2003_03
ORD IDord-a8e322212cca4659b7c8f8ded7c21c3a
Source noteuspto-grants-2003_03