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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181562Generated: November 2, 2026

4-Aminophenol → HCID 135839313, compound

https://huagongshe.com/reaction/2181562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantDimethylformamideHCID 6228—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant1H-indazole-6-carboxylic acidHCID 16227938—
CatalystTriethylamineHCID 8471—
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 title compound was isolated as a solid (20 mg). 1H NMR (methanol-d4) 56.87 (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 numberUS06891044B2
Source datasetuspto-grants-2005_05
ORD IDord-d6585ba34a624a469397457877ce3b2d
Source noteuspto-grants-2005_05