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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DiphenylethylamineHCID 77575—
ReactantDiisopropylethylamineHCID 81531—
Reactant(1S,2R,3S,5R)-3-(di-tert-butoxycarbonylamino)-5-(2,6-dichloro-purin-9-yl)-cyclopentane-1,2-diolHCID 57777515—
SolventTetrahydrofuranHCID 8028—
Product{2-Chloro-9-[(1R,4S)-4-(di-Boc-amino)-cyclopent-2-enyl]-9H-purin-6-yl}-(2,2-diphenyl-ethyl)amineHCID 59418857—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188100B2
Source datasetuspto-grants-2012_05
ORD IDord-bf85e62ed3cf468cbdb9a8afd9d9cbf7
Source noteuspto-grants-2012_05