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Updated: May 10, 2026

Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
rac-5-(1-Methyl-eth-yl)-2-sulfanylidene-imidazolidin-4-one
Rosane de P Castro1, Fernando C Macedo, Tiago O Brito
1Instituto de Física - UFG, Caixa Postal 131, 74001-970 Goiânia, GO, Brazil.
Abstract:
In the title compound, C6H10N2OS, the 2-sulfanylideneimidazolidin-4-one fragment is essentially planar (r.m.s. deviation = 0.0033 Å). In the crystal, one amino group is involved in N-H⋯O hydrogen bonding, which links pairs of mol-ecules into inversion dimers, while the other amino group generates weak N-H⋯S hydrogen bonds, which link these dimers into chains in [10-1]. The chains are further aggregated into layers parallel to the ac plane through weak C-H⋯O inter-actions.
