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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39344Generated: October 29, 2026

Methylamine → (R)-5-cyclopentyl-4-ethyl-N-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridin-7-amine

https://huagongshe.com/reaction/39344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTrifluoroacetic acidHCID 6422—
ReactantCarbonate IonHCID 19660—
Reactant(R)-7-chloro-5-cyclopentyl-4-ethyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridineHCID 59389586—
SolventEthanolHCID 702—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product(R)-5-cyclopentyl-4-ethyl-N-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridin-7-amineHCID 2488822561%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a vial containing (R)-7-chloro-5-cyclopentyl-4-ethyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridine (70 mg, 0.23 mmol) was added a solution of methylamine in ethanol (2 mL, 2M soln.) The vessel was sealed then heated at 50° C. for 18 hours. After cooling, the solvent was removed under reduced pressure and the crude product was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 M, 100 Å column, gradient 10%-95% B (solvent A: 0.05% TFA in water; solvent B: CH3CN) over 16 minutes at 25 mL/min]. The free base was obtained by passing the TFA salt in acetonitrile/water through a carbonate cartridge to afford the title compound as a white powder (42 mg, 61% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524902B2
Source datasetuspto-grants-2013_09
ORD IDord-e9d3f5a185254435852a078380e36718
Source noteuspto-grants-2013_09