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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441223Generated: November 2, 2026

Cyclopentylamine → (9-{(4S,1R,2R,5R)-4-[(2-fluorophenylthio)methyl]-7,7-dimethyl-3,6,8-trioxabicyclo[3.3.0]oct-2-yl}purin-6-yl)cyclopentylamine

https://huagongshe.com/reaction/1441223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantHCID 86587415HCID 86587415—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
Product(9-{(4S,1R,2R,5R)-4-[(2-fluorophenylthio)methyl]-7,7-dimethyl-3,6,8-trioxabicyclo[3.3.0]oct-2-yl}purin-6-yl)cyclopentylamineHCID 67190843—

Reaction Steps

To a solution of 1-{[(2S,1R,4R,5R)-4-(6-chloropurin-9-yl)-7,7-dimethyl-3,6,8-trioxabicyclo[3.3.0]oct-2-yl]methylthio}-2-fluorobenzene, a compound of formula (3), (0.125 g, 2.86 mmoles) in 10 mL of ethanol and 1 mL of triethylamine was added cyclopentylamine in excess, and the mixture refluxed under nitrogen for 24 hours. The solvent was removed under reduced pressure, and the residue was purified by preparative TLC using 1:1 EtOAc:Hexanes to give (9-{(4S,1R,2R,5R)-4-[(2-fluorophenylthio)methyl]-7,7-dimethyl-3,6,8-trioxabicyclo[3.3.0]oct-2-yl}purin-6-yl)cyclopentylamine, a compound of formula (4), as a yellow oil (80 mg, 56%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655638B2
Source datasetuspto-grants-2010_02
ORD IDord-8e93ddc7dba74b19845d250375310de7
Source noteuspto-grants-2010_02