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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901517Generated: November 1, 2026

HCID 22854555, compound → HCID 10022940, compound

https://huagongshe.com/reaction/1901517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22854555HCID 22854555—
SolventAmmoniaHCID 222—
ProductHCID 10022940HCID 1002294057%

Reaction Steps

The above 2',3',5'-tri-O-benzoyl-2-chloro-N-(1-piperidinyl)adenosine (19.2 g, 27.5 mmol) was dissolved in methanolic ammonia (150 ml) (previously saturated at -10° C.) and stirred at room temperature for 18 hours. The precipitated benzamide was removed by filtration, and the filtrate was evaporated to a fawn oil, which was triturated with diethyl ether to provide the title compound (6.0 g, 57%) as a white foam, 1H NMR (400 MHz, Me2SO-d6) δ 3.55 (1H, m, H-5'a), 3.66 (1H, m, H-5'b), 3.94 (1H, q, H-4'), 4.12 (1H, m, H-3'), 4.50 (1H, q, H-2'), 5.82 (1H, d, H-1'), 8.40 (1H, s, H-8); HPLC retention time 26.57 (gradient elution, 5-25% acetonitrile/0.1M pH 3.3 ammonium sulphate buffer: 214 nm detector); purity 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578582
Source datasetuspto-grants-1996_11
ORD IDord-1326650c45cc4db581cc1b52335b7791
Source noteuspto-grants-1996_11