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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861126Generated: November 3, 2026

4-Aminophenol → HCID 135839313, compound

https://huagongshe.com/reaction/1861126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant319474-36-7HCID 135839310—
CatalystTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
ProductHCID 135839313HCID 135839313—

Reaction Steps

To a solution of 3-(1H-benzoimidazol-2-yl)-1H-indazole-6-carboxylic acid (208 mg, 0.7 mmol) in dry dimethylformamide (6 mL) was added 4-aminophenol (82 mg, 0.7 mmol) followed by HATU (312 mg, 0.8 mmol) and then triethylamine (20 drops) was added. The reaction was stirred overnight at room temperature. LC/MS showed desired product as major component. The solvent was removed by vacuum. The residue remaining was taken up in water and ethyl acetate. The layers were separated and the organic layer was concentrated under vacuum. The residue was dissolved in methanol (10 mL) and half of this solution was purified by HPLC using a gradient of 5% acetonitrile/water to 55% acetonitrile/water over 60 minutes with 0.1% trifluoroacetic acid in the water. The tide compound was isolated as a solid (20 mg). 1H NMR (methanol-d4) δ 6.87 (2H, d, 8.8 Hz), 7.55 (2H, d, 8.7 Hz), 7.61 (2H, m), 7.87 (2H, br s), 8.00 (1H, d, 8.4 Hz), 8.35 (1H, s), 8.52 (1H, d, 8.6 Hz). MS (APCI pos) 370.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531491B1
Source datasetuspto-grants-2003_03
ORD IDord-361d268f0075405ea46552286af21f28
Source noteuspto-grants-2003_03