Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | 2004-07-1 | HCID 102197 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10959042 | HCID 10959042 | — |
Reaction Steps
To suspension of (4S,2R,3R,5R)-2-[2-amino-6-chloro-purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol in 15 mL of ethanol was added 0.4 g of cyclopentyl amine and 10 mmol of trimethyl amine. The mixture was stirred at 80° C. for 24 hours. The residue was purified using preparative thin layer chromatography (15:1 dichloromethane:methanol) to yield (4S,2R,3R,5R)-2-[2-amino-6-(cyclopentylamino)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol, a compound of formula (8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381714B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-dff332c8c27b47eca824a149021d7b14 |
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| Source note | uspto-grants-2008_06 |
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