Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518241Generated: November 1, 2026

Ammonium Hydroxide → HCID 71269970, compound

https://huagongshe.com/reaction/518241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 86677059HCID 86677059—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71269970HCID 71269970—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of (S)-3-(1-((2-chloro-5-iodopyrimidin-4-yl)amino)ethyl)-8-(2-methoxypyrimidin-5-yl)-2-phenylisoquinolin-1 (2H)-one 3 (800 mg, 1.31 mmol) in anhydrous 1,4-dioxane (4 mL) in a sealed tube, ammonium hydroxide (7 mL) was added and the resulting mixture was stirred at 110° C. for 20 h. The mixture was allowed to cool to RT, quenched with water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by ISCO column chromatography using a silica gel cartridge and eluting with 0-8% MeOH-DCM to afford the product, (S)-3-(1-((2-amino-5-iodopyrimidin-4-yl)amino)ethyl)-8-(2-methoxypyrimidin-5-yl)-2-phenylisoquinolin-1(2H)-one 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115141B2
Source datasetuspto-grants-2015_08
ORD IDord-992334d313124daabe7b31cb93a6f9e0
Source noteuspto-grants-2015_08