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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713333Generated: November 2, 2026

8-[3'-(3-Aminopropoxy)biphenyl-4-ylmethylamino]-adenosine → HCID 178512989, compound

https://huagongshe.com/reaction/1713333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-[3'-(3-Aminopropoxy)biphenyl-4-ylmethylamino]-adenosineHCID 59460473—
ReactantN-(Carbobenzoxy)-1H-pyrazole-1-carboxamidineHCID 137319688—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178512989HCID 17851298923.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

8-[3′-(3-Aminopropoxy)biphenyl-4-ylmethylamino]-adenosine (0.2 g) was suspended in tetrahydrofuran (2 mL), N-benzyloxycarbonyl-1H-pyrazole-1-carboxamidine (0.47 g) was added, and the resulting mixture was stirred at 60° C. for 24 hours. The reaction mixture was concentrated under reduced pressure and the residue obtained was purified by column chromatography on aminopropylated silica gel (eluent: ethyl acetate/methanol=8/1-6/1). A mixture of the compound obtained and 10% palladium on carbon (43.8 wt % H2O, 0.05 g) in methanol (2 mL) was stirred at room temperature for 4 hours under a hydrogen atmosphere. The insoluble material was filtered out and the filtrate was concentrated under reduced pressure to give the title compound (0.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795236B2
Source datasetuspto-grants-2010_09
ORD IDord-ba7e6f675c2748ae87111646fa9e88b1
Source noteuspto-grants-2010_09