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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242478Generated: October 26, 2026

Hydrochloric Acid → HCID 178472218, compound

https://huagongshe.com/reaction/2242478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 1-(6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-9H-purin-2-yl)-1H-pyrazole-4-carboxylateHCID 9865974—
Reactant2-HydrazinoadenosineHCID 10357262—
ReactantEthyl 2-formyl-3-oxopropanoateHCID 11029955—
SolventEthanolHCID 702—
ProductHCID 178472218HCID 178472218—

Reaction Conditions

Temperature10 °C

Reaction Steps

A reaction vessel is charged with 2-hydrazinoadenosine (450 g) and absolute ethanol (11376 g). HCl (7.47 g) and ethyl 2-formyl-3-oxopropionate (1557 g) are added. The mixture is heated to reflux and sampled until the level of residual 2-hydrazinoadenosine in the mixture is not more than 0.50% and the level of the compound of formula (3) is not more than 2.5%. The mixture is slowly cooled to approximately 10° C. The product, the compound of formula (4) is isolated by filtration and washed with absolute ethanol (5121 g). The product is dried under vacuum at up to 40° C. until residual ethanol is not more than 5000 ppm to give ethyl (2E)-3-({9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-[4-(ethoxycarbonyl)-pyrazolyl]purin-6-yl}amino)-2-formylprop-2-enoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671192B2
Source datasetuspto-grants-2010_03
ORD IDord-3d29700967b14b699c0cf98ca0cb5e0f
Source noteuspto-grants-2010_03