1-Trimethylsilyltetrazole, 1, has been synthesised from chlorotrimethylsilane and tetrazole in the presence of triethylamine as an auxiliary base. The structure of this compound has been determined in the crystalline phase by X-ray diffraction of a crystal grown in situ. The gas-phase structures of 1 and 1-trimethylsilyl-1,2,4-triazole, 2, have been determined by gas-phase electron diffraction ...

Rationale. The goal of antihypertensive treatment is to reduce risk of cardiovascular morbidity and mortality. Apart from blood pressure lowering per se, also reducing the activities of the renin-angiotensin system and sympathetic nervous system appears to be important. Angiotensin II receptor blocker drugs (ARBs) have provided a useful class of anti-hypertensive drugs. Eprosartan is a relative...

Driven by an interest in the impact of para-substituent calix[4]arenes on metal complexation and structural chemistry, studies p-cyclohexylcalix[4]arene (L) have been carried out. The 1:1 dichloromethane dimethylformamide solvates were found to be isostructural, different typical bilayer structure often observed for p-t-butylcalix[4]arene solvates. methanol solvate, contrast, does form a bilaye...

Magnetic nanoparticle-supported sulfanilic acid (MNPs-PhSO3H) has been used as an efficient catalyst for the preparation of 1,4-diazepines containing tetrazole ring. The catalyst has been characterized by FT-IR (Fourier-transform infrared spectroscopy), SEM (scanning electron microscope), XRD (X-ray diffraction) and VSM (vibrating-sample magnetometer). The present synthetic protocol provides se...

An efficient method for the preparation of 5-substituted 1H-tetrazole derivatives is reported using MoO3-SiO2 as an efficient heterogeneous catalyst. This method has the advantages of high yields, simple methodology and easy work-up. This catalyst could be recycled very easily, which makes this methodology environmentally benign.

[reaction: see text] Organocatalytic asymmetric Mannich reaction of protected amino ketones with imines in the presence of an L-proline-derived tetrazole catalyst afforded diamines with excellent yields and enantioselectivities of up to 99%. The amino ketone protecting group controlled the regioselectivity of the reaction providing access to chiral 1,2-diamines from azido ketones and 1,4-diamin...

The title compound, C(9)H(7)N(5), was synthesized by reaction of 4-(bromomethyl)benzonitrile and 2H-tetrazole in the presence of KOH. The relative orientation of the planar tetra-zole ring and the methyl-benzonitrile moiety is (-)-anti-clinal. The crystal packing is dominated by van der Waals inter-actions.