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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 8-[3'-(3-Aminopropoxy)biphenyl-4-ylmethylamino]-adenosine | HCID 59460473 | — |
| Reactant | N-(Carbobenzoxy)-1H-pyrazole-1-carboxamidine | HCID 137319688 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178512989 | HCID 178512989 | 23.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795236B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-ba7e6f675c2748ae87111646fa9e88b1 |
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| Source note | uspto-grants-2010_09 |
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