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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216279Generated: November 1, 2026

Triphenylphosphine → (5-Aminomethyl-2-chloro-pyrimidin-4-yl)-(2,2-dimethyl-propyl)-amine 2HCl

https://huagongshe.com/reaction/2216279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(5-Azidomethyl-2-chloro-pyrimidin-4-yl)-(2,2-dimethyl-propyl)-amineHCID 21941878—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(5-Aminomethyl-2-chloro-pyrimidin-4-yl)-(2,2-dimethyl-propyl)-amine 2HClHCID 21941877—

Reaction Steps

A solution of 1.47 g (15.77 mmol) (5-azidomethyl-2-chloro-pyrimidin-4-yl)-(2,2-dimethyl-propyl)-amine and 1.67 g (6.35 mmol) of triphenylphosphine in 20 ml of THF and 0.08 ml of H2O is stirred at r.t. for 24 h. Then the solvent is removed and the residue dissolved in 40 ml EtOH and 17 ml NH3 (25%). This reaction mixture is stirred for 48 h at r.t. and again the solvent is removed. The residue is dissolved in diethylether and twice extracted with 25 ml of 1N HCl. Both acidic extracts were combined and once more extracted with diethylether, then the acidic layer is evaporated under vacuo. The solid residue was triturated with diethylether yielding (5-Aminomethyl-2-chloro-pyrimidin-4-yl)-(2,2-dimethyl-propyl)-amine 2HCl as slightly yellow crystalls.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112589B2
Source datasetuspto-grants-2006_09
ORD IDord-1318c320f7ff447593a598f453c6e2e1
Source noteuspto-grants-2006_09