uldazepam

Uldazepam is a drug which is a benzodiazepine derivative. It has sedative and anxiolytic effects similar to those of other benzodiazepines.

In the Vinony graph

Within Vinony's link graph, uldazepam is referenced by 540 other articles, and connects out to benzodiazepine drug, alphenal and zapizolam.

It sits within the topics 2-Chlorophenyl compounds, Allyl compounds and Benzodiazepines.

Its subject is documented across 8 Wikipedia language editions.

Chemical data

Formula: C18H15Cl2N3O
Molecular weight: 360.2 g/mol
IUPAC name: 7-chloro-5-(2-chlorophenyl)-N-prop-2-enoxy-3H-1,4-benzodiazepin-2-amine
SMILES: C=CCONC1=NC2=C(C=C(C=C2)Cl)C(=NC1)C3=CC=CC=C3Cl
InChIKey: DTMPGSXFUXZBDK-UHFFFAOYSA-N
XLogP: 3.9
Polar surface area: 46 Å²
H-bond donors: 1
H-bond acceptors: 3
Formal charge: 0

via PubChem

Drug data · ChEMBL

Max clinical phase: Phase 2
Molecule type: Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of: chemical compound
Mass: 359.059

Show 3 more facts

chemical formula: C₁₈H₁₅Cl₂N₃O
canonical SMILES: C=CCONC1=NC2=C(C=C(C=C2)Cl)C(=NC1)C3=CC=CC=C3Cl
Commons category: Uldazepam

Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

3 sections

Contents

Synthesis
See also
References

Uldazepam is a drug which is a benzodiazepine derivative. It has sedative and anxiolytic effects similar to those of other benzodiazepines.

==Synthesis== Thio thionamide is even more prone to amidine formation than the lactam itself. thumb|center|700px|Uldazepam synthesis: J. B. Hester, Jr., (1970); Chem. Abstr., 73: 99,001t (1970). Reaction of thionamide (2) with O-allyl-hydroxylamine gave the oximino (3) uldazepam.

Excerpted from Wikipedia’s “uldazepam” article, available under the CC BY-SA 4.0 licence.