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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061718Generated: November 3, 2026

Ethylenediamine → 2-(2-Aminoethyl)-1,3-di-Boc-guanidine

https://huagongshe.com/reaction/1061718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantN,N'-Bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidineHCID 4428040—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Aminoethyl)-1,3-di-Boc-guanidineHCID 10990304—

Reaction Steps

With continued reference to Scheme J, a solution of the N,N′-bis-(Boc)-1H-Pyrazole-1-carboxamidine (2 g, 6.45 mmol) in THF (50 ml) was added dropwise to ethylene diamine (4 ml, 59.6 mmol) in THF (100 ml). After 30 min of mixing at room temperature solvent was evaporated then toluene (100 ml) was added and evaporated in order to remove remaining traces of the ethylene diamine. The resulting product (Compound XXIV) was treated immediately according to scheme K since it decomposes at room temperature. 1H NMR (CDCl3, 400 MHz) δ 1.40-1.61 (m, 18H), 2.87-2.90 (t, 2H,), 3.47-3.50 (m, 2H), 6.31-6.34 (t, 0.61H), 7.61-7.62 (d, 1H), 8.45-8.66 (broad s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960594B2
Source datasetuspto-grants-2005_11
ORD IDord-d313c438859e41a984e2dbc8b1c7a778
Source noteuspto-grants-2005_11