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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038164Generated: November 2, 2026

Phenylmethyl 2-{3-[6-amino-2-(butyloxy)-8-(methyloxy)-9H-purin-9-yl]propyl}-1-piperidinecarboxylate → 2-(Butyloxy)-8-(methyloxy)-9-[3-(2-piperidinyl)propyl]-9H-purin-6-amine

https://huagongshe.com/reaction/2038164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylmethyl 2-{3-[6-amino-2-(butyloxy)-8-(methyloxy)-9H-purin-9-yl]propyl}-1-piperidinecarboxylateHCID 58306132—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(Butyloxy)-8-(methyloxy)-9-[3-(2-piperidinyl)propyl]-9H-purin-6-amineHCID 5830618477.9%

Reaction Steps

Phenylmethyl 2-{3-[6-amino-2-(butyloxy)-8-(methyloxy)-9H-purin-9-yl]propyl}-1-piperidinecarboxylate (for example, as prepared for Intermediate 11) (1.16 g, 2.336 mmol) in ethanol (130 mL) was hydrogenated over 10% palladium on carbon (0.497 g, 0.467 mmol) at ambient temperature overnight. The mixture was filtered through a Celite cartridge under nitrogen, washed with ethanol and evaporated in vacuo to give the title compound as a cream solid (0.66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575340B2
Source datasetuspto-grants-2013_11
ORD IDord-40e9dd0af5854dbb8f5ba193b79c1a81
Source noteuspto-grants-2013_11