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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013652Generated: October 31, 2026

4-Aminophenol → HCID 135964711, compound

https://huagongshe.com/reaction/1013652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 11184602HCID 11184602—
SolventDichloromethaneHCID 6344—
Solvent(+-)-2-ButanolHCID 6568—
ProductHCID 135964711HCID 135964711—

Reaction Steps

A mixture of 4-aminophenol (42 mg, 0.38 mmol), 1-chloro-4-(4-methylpiperazin-1-yl)phthalazine (100 mg, 0.381 mmol), and TFA (29 μl, 0.38 mmol) was heated in 2-butanol (3 mL) in a sealed tube at 90° C. overnight. Next day LC/MS shows completion of reaction. The reaction was cooled and diluted with DCM. Aqueous sodium bicarbonate was added and the organic layer was collected. The aqueous layer was neutralized with 1N HCl and the product was extracted with DCM. The organic layers were combined, dried over sodium sulfate, and concentrated to afford 4-(4-(4-methylpiperazin-1-yl)phthalazin-1-ylamino)phenol as solid brown material. MS [M+H]=336.2. Calc'd for C19H21N5O: 335.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-5f497908eb58472bb6ee22a77a2c308d
Source noteuspto-grants-2011_07