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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976562Generated: November 1, 2026

HCID 178490826, compound → HCID 178490829, compound

https://huagongshe.com/reaction/1976562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178490826HCID 178490826—
CatalystPalladiumHCID 23938—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 178490829HCID 17849082977.4%

Reaction Steps

A solution of the above 6-amino-3-(3-benzyloxy-4-methoxy-benzyl)-8-(1-benzyloxy-1-methyl-ethyl)-3H-purine hydrochloride (3.22 g) in THF:methanol (1:1) (60 ml) was hydrogenated at room temperature and pressure for 2.5 hours with 10% Pd-C (0.64 g). The catalyst was filtered off and the solution evaporated to dryness in vacuo. The residue was crystallized from acetone to give 6-amino-3-(3-hydroxy-4-methoxy-benzyl)-8-(1-hydroxy-1-methyl-ethyl)-3H-purine hydrochloride, (1.67 g, 77.3%) mp 155-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06228859B1
Source datasetuspto-grants-2001_05
ORD IDord-c004834fde6649989afe394aaff1d68e
Source noteuspto-grants-2001_05