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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456042Generated: November 1, 2026

Methanesulfonic Acid → HCID 86750597, compound

https://huagongshe.com/reaction/1456042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
ReactantBoron tribromideHCID 25134—
ReactantHCID 19592238HCID 19592238—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 86750597HCID 8675059737.9%

Reaction Steps

A mixture of 1-ethyl-6-methoxy-N-(4-methoxyphenylmethyl)-1H-pyrazolo[3,4-b]quinolin-4-amine (1.0 g, 2.76 mmol), boron tribromide (6 mL, 6 mmol) and 1,2-ethylenedichloride (30 mL) was stirred at room temperature overnight. The reaction mixture was poured into water and then was basified with NaOH. The layers were separated and then the aqueous layer was acidified with acetic acid. The precipitate which formed was collected by filtration, washed with water and dried to afford the product as the free base. The free base was taken up in methanol and treated with methanesulfonic acid. The methanol was evaporated and the solid residue was recrystallized from 2-propanol/methanol/ether and dried in vacuo to afford 350 mg of 1-ethyl-6-hydroxy-N-(4-hydroxyphenyl methyl)-1H-pyrazolo[3,4-b]quinolin-4-amine.CH3SO3H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843956
Source datasetuspto-grants-1998_12
ORD IDord-e24ec5625b2645f3af745f63356152ec
Source noteuspto-grants-1998_12