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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217132Generated: October 31, 2026

Sodium Bicarbonate → HCID 178423750, compound

https://huagongshe.com/reaction/217132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69033406HCID 69033406—
ReactantHCID 178423764HCID 178423764—
SolventEthanol hydrochlorideHCID 21887872—
ProductHCID 178423750HCID 17842375094%
ProductHCID 178423764HCID 178423764—

Reaction Steps

3-(1-(2-Fluoro-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-ylamino)ethyl)-8-methyl-2-phenylisoquinolin-1(2H)-one (compound 5203) (160 mg, 0.32 mmol) was dissolved in HCl/EtOH (3 M, 5 mL) and the resulting mixture was stirred at room temperature for 1 h. The mixture was neutralized with saturated NaHCO3 aqueous solution to pH=7-8, and extracted with CH2Cl2 (50 mL×3). The combined organic layer was washed with brine, dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was recrystallized from ethyl acetate and hexanes. The solid was collected by filtration and dried in vacuo to afford the desired product, 3-(1-(2-fluoro-9H-purin-6-ylamino)ethyl)-8-methyl-2-phenylisoquinolin-1(2H)-one (compound 5204) (125 mg, 94% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193182B2
Source datasetuspto-grants-2012_06
ORD IDord-c72e2f0c9e424aaeb5d0eeeee5b6d99b
Source noteuspto-grants-2012_06