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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887041Generated: November 1, 2026

Hydrochloric Acid → tert-butyl 3-(6-amino-8-oxo-7H-purin-9(8H)-yl)phenylcarbamate

https://huagongshe.com/reaction/1887041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-Butyl 3-(6-(dibenzylamino)-8-oxo-7H-purin-9(8H)-yl)phenylcarbamateHCID 86691210—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Producttert-butyl 3-(6-amino-8-oxo-7H-purin-9(8H)-yl)phenylcarbamateHCID 8669121276.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of tert-butyl 3-(6-(dibenzylamino)-8-oxo-7H-purin-9(8H)-yl)phenylcarbamate (4) (3.0 g, 5.7 mmol) in 120 mL MeOH was added 3.0 g Pd(OH)2/C (20 wt %) and 6 drops of con. HCl. After two vacuum/H2 cycles to remove air from the reaction flask, the stirred mixture was heated at 60° C. under hydrogen atmosphere overnight. The reaction mixture was filtered through a Celite pad and the filtrate was concentrated to dryness in vacuo. The residue was purified by column chromatography (silica gel, 0 to 5% methanol in DCM) to give tert-butyl 3-(6-amino-8-oxo-7H-purin-9(8H)-yl)phenylcarbamate (5) (1.5 g, 76%) as a white solid. LC-MS (ESI): m/z (M+1) 343.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501724B1
Source datasetuspto-grants-2013_08
ORD IDord-b97a36d0c15943a6aac5d6f0855c700c
Source noteuspto-grants-2013_08