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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709946Generated: November 1, 2026

Sodium Carbonate → HCID 178514853, compound

https://huagongshe.com/reaction/709946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBis(adamantan-1-yl)(butyl)phosphaneHCID 11371790—
Reactant1H-Pyrazole-4-boronic acidHCID 17750278—
ReactantHCID 178461883HCID 178461883—
Catalystpalladium(II) acetateHCID 167845—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178514853HCID 178514853—

Reaction Conditions

Temperature160 °C

Reaction Steps

(S)-3-(14(9H-purin-6-yl)amino)ethyl)-8-chloro-2-phenylisoquinolin-1(2H)-one (3) (200 mg, 0.48 mmol) and 1H-pyrazole-4-boronic acid (108 mg, 0.96 mmol) were dissolved in anhydrous NMP (8 mL) and the resulting solution was degassed and back-filled with argon (two cycles). To this mixture, Na2CO3 (152 mg, 1.44 mmol), Pd(OAc)2 (22 mg, 0.096 mmol) and di-(1-adamantyl)-n-butylphosphine (104 mg, 0.288 mmol) were added sequentially. The resulting mixture was degassed and back-filled with argon (two cycles) and then stirred at 160° C. under argon for 3 h. The reaction mixture was allowed to cool to RT and then partitioned between water and ethyl acetate. The organic layer was separated and the aqueous layer was 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 triturated with Et2O to afford the product, (S)-3-(14(9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-3-yl)isoquinolin-1(2H)-one (6) as a yellowish solid. ESI-MS m/z: 449.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181221B2
Source datasetuspto-grants-2015_11
ORD IDord-bddf28d2e8d34a99bf374b0e74106120
Source noteuspto-grants-2015_11