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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910883Generated: October 30, 2026

Sodium Carbonate → HCID 178435781, compound

https://huagongshe.com/reaction/1910883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTributylvinyltinHCID 81998—
ReactantBis(adamantan-1-yl)(butyl)phosphaneHCID 11371790—
ReactantHCID 178461883HCID 178461883—
Catalystpalladium(II) acetateHCID 167845—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178435781HCID 178435781—

Reaction Conditions

Temperature160 °C

Reaction Steps

(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-8-chloro-2-phenylisoquinolin-1(2H)-one (3) (417 mg, 1.0 mmol) and tributyl(vinyl)tin (0.58 mL, 2.0 mmol) were dissolved in anhydrous NMP (10 mL) and the resulting solution was degassed and back-filled with argon (two cycles). To this mixture, Na2CO3 (212 mg, 2.0 mmol), Pd(OAc)2 (45 mg, 0.2 mmol) and di-(1-adamantyl)-n-butylphosphine (215 mg, 0.6 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 1 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 purified by ISCO (silica gel cartridge, 0-10% MeOH-DCM) to afford the product, (S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-vinylisoquinolin-1(2H)-one (8) as an off-while solid. ESI-MS m/z: 409.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604032B2
Source datasetuspto-grants-2013_12
ORD IDord-064cbf2256f44c93ad28f84c20b77295
Source noteuspto-grants-2013_12