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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920667Generated: October 30, 2026

4-(2-(Butylamino)-5-(4-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidin-7-yl)cyclohex-3-enol → HCID 178448859, compound

https://huagongshe.com/reaction/920667

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-(Butylamino)-5-(4-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidin-7-yl)cyclohex-3-enolHCID 86731158—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178448859HCID 178448859—

Reaction Steps

A mixture of 4-(2-(butylamino)-5-(4-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidin-7-yl)cyclohex-3-enol (0.095 g, 0.25 mmol) and Pd/C (0.01 g, 10 wt %) in 5 mL MeOH was stirred under H2 atmosphere for 3 h. After filter through a plug of celite, the filtrate was concentrated and purified by Prep-HPLC. The cis-4-(2-(butylamino)-5-(4-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidin-7-yl)cyclohexanol was obtained as the major product (0.040 g). The trans-4-(2-(butylamino)-5-(4-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidin-7-yl)cyclohexanol was co-elute with 4-(2-(butylamino)-5-(4-fluorophenyl)-6,7-dihydro-5H-pyrrolo[3,2-d]pyrimidin-7-yl)cyclohexanol (0.035 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273056B2
Source datasetuspto-grants-2016_03
ORD IDord-4592cee720074a11a2b6569ab919a60d
Source noteuspto-grants-2016_03