HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215850Generated: October 29, 2026
3-Pentanamine → {(1S,4R)-4-[2-Chloro-6-(1-ethyl-propylamino)-purin-9-yl]-cyclopent-2-enyl}-propionyl-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/215850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pentanamine | HCID 12019 | — |
| Reactant | [(1S,4R)-4-(2,6-Dichloro-purin-9-yl)-cyclopent-2-enyl]-propionyl-carbamic acid tert-butyl ester | HCID 86622633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {(1S,4R)-4-[2-Chloro-6-(1-ethyl-propylamino)-purin-9-yl]-cyclopent-2-enyl}-propionyl-carbamic acid tert-butyl ester | HCID 86622634 | — |
Reaction Steps
[(1S,4R)-4-(2,6-Dichloro-purin-9-yl)-cyclopent-2-enyl]-propionyl-carbamic acid tert-butyl ester (700 mg, 1.64 mmol) is dissolved in THF (15 mL) under an atmosphere of argon. 3-Pentylamine (315 mg, 3.61 mmol) is added and the reaction mixture is stirred at 50° C. The reaction is shown to be complete by LCMS after 18 hours. The reaction mixture is partitioned between DCM (50 mL) and 0.1 M HCl (50 mL). The organic layer is washed with water (20 mL) and brine (20 mL), dried over MgSO4, filtered and the solvent is removed in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193164B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-f716b118d60d46218329522b6fe4afe7 |
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| Source note | uspto-grants-2012_06 |
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