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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223168Generated: November 1, 2026

1-Methoxyethanol → HCID 135409288, compound

https://huagongshe.com/reaction/223168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethoxyethanolHCID 3015637—
ReactantHCID 22821688HCID 22821688—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 135409288HCID 135409288—

Reaction Steps

A mixture of 8.0 g of 2-amino-4-allyloxy-7-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine, 1.5 g of 20% palladium on charcoal, 6.7 ml of acetic acid, and 150 ml of methoxy ethanol is hydrogenated at 50° C. and approximately 3 atmospheres until the uptake of hydrogen ceases. The mixture is filtered, evaporated in vacuo, dissolved in water, and treated with 60 ml of wet IR-45 ion exchange resin. The filtrate is concentrated to dryness in vacuo and the residue is recrystallized from water to provide pure 2-amino-7-β-D-arabinofuranosyl-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352795
Source datasetuspto-grants-1982_10
ORD IDord-7246a0cd86f5402d9ca0f0b7431c2cd6
Source noteuspto-grants-1982_10