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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186253Generated: October 31, 2026

Hydrochloric Acid → methyl (3-{[[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl](3-morpholin-4-ylpropyl)amino]methyl}phenyl)acetate monohydrochloride

https://huagongshe.com/reaction/1186253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAzd-8848HCID 11592228—
SolventMethanolHCID 887—
Productmethyl (3-{[[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl](3-morpholin-4-ylpropyl)amino]methyl}phenyl)acetate monohydrochlorideHCID 44128977—

Reaction Conditions

Temperature60 °C

Reaction Steps

A 80 mM solution of hydrochloric acid in methanol (65.0 μl, 5.2 μmol) was added to a solution of methyl (3-{[[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl](3-morpholin-4-ylpropyl)amino]methyl}phenyl)acetate (3.0 mg, 5.3 μmol) dissolved in methanol (1.5 ml) at room temperature. The solution was shaken at 60° C. for one hour, then cooled to 5° C. After 30 minutes, the solvent was left to slowly evaporate at 5° C., to give methyl (3-{[[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl](3-morpholin-4-ylpropyl)amino]methyl}phenyl)acetate monohydrochloride as the final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673907B2
Source datasetuspto-grants-2014_03
ORD IDord-efff998cdcce4b7a8b86e23083057eb1
Source noteuspto-grants-2014_03