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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | (R)-7-chloro-5-cyclopentyl-4-ethyl-4,5-dihydro-[1,2,4]triazolo[4,3-f]pteridine | HCID 59389586 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile--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-amine | HCID 24888225 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524902B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-e9d3f5a185254435852a078380e36718 |
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| Source note | uspto-grants-2013_09 |
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