HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929765Generated: November 3, 2026
2,2-Diphenylethylamine → {2-Chloro-9-[(1R,4S)-4-(di-Boc-amino)-cyclopent-2-enyl]-9H-purin-6-yl}-(2,2-diphenyl-ethyl)amine
https://huagongshe.com/reaction/1929765
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2-Diphenylethylamine | HCID 77575 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (1S,2R,3S,5R)-3-(di-tert-butoxycarbonylamino)-5-(2,6-dichloro-purin-9-yl)-cyclopentane-1,2-diol | HCID 57777515 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {2-Chloro-9-[(1R,4S)-4-(di-Boc-amino)-cyclopent-2-enyl]-9H-purin-6-yl}-(2,2-diphenyl-ethyl)amine | HCID 59418857 | — |
Reaction Steps
(1S,2R,3S,5R)-3-(di-Boc-amino)-5-(2,6-dichloro-purin-9-yl)-cyclopentane-1,2-diol (13.0 g, 27.66 mmol) is dissolved in THF (250 mL) under an atmosphere of argon. DIPEA (4.28 g, 33.19 mmol) is added followed by 2,2-diphenylethylamine (6.0 g, 30.43 mmol) and the reaction mixture is stirred at 50° C. The reaction is shown to be complete by LCMS after 18 hours. The solvent is removed in vacuo and the reaction mixture is partitioned between dichloromethane (250 mL) and 0.1 M HCl (250 mL). The organic layer is washed with water (200 mL) and brine (200 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 | US08188100B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-bf85e62ed3cf468cbdb9a8afd9d9cbf7 |
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| Source note | uspto-grants-2012_05 |
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