Title: Benazepril
CAS Registry Number: 86541-75-5
CAS Name: (3
S)-3-[[(1
S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1
H-1-benzazepine-1-acetic acid
Synonyms: (3
S)-1-(carboxymethyl)-[[(1
S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-1
H-[1]benzazepin-2-one; (3
S)-3-[[(1
S)-1-carboxy-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1
H-1-benzazepine-1-acetic acid 3-ethyl ester
Molecular Formula: C24H28N2O5
Molecular Weight: 424.49
Percent Composition: C 67.91%, H 6.65%, N 6.60%, O 18.85%
Literature References: Angiotensin converting enzyme (ACE) inhibitor. Hydrolyzed
in vivo to the active diacid metabolite. Prepn: J. W. H. Watthey,
EP 72352;
idem, US 4410520 (both 1983 to Ciba-Geigy); J. W. H. Watthey
et al., J. Med. Chem. 28, 1511 (1985). Clinical pharmacology: M. D. Schaller
et al., Eur. J. Clin. Pharmacol. 28, 267 (1985). GC-MS determn in plasma and urine: A. Sioufi
et al., J. Chromatogr. 434, 239 (1988). Pharmacokinetics of benazepril and benazeprilat: G. Kaiser
et al., Biopharm. Drug Dispos. 10, 365 (1989). Multicenter clinical trial in hypertension: M. Moser
et al., ibid. 49, 322 (1991); in congestive heart failure: H. T. Colfer
et al., Am. J. Cardiol. 70, 354 (1992).
Properties: mp 148-149°. [a]D -159° (c = 1.2 in ethanol).
Melting point: mp 148-149°
Optical Rotation: [a]D -159° (c = 1.2 in ethanol)
Derivative Type: Hydrochloride
CAS Registry Number: 86541-74-4
Manufacturers' Codes: CGS-14824A
Trademarks: Briem (Fabre); Cibacen (Novartis); Fortekor (Novartis); Lotensin (Novartis)
Molecular Formula: C24H28N2O5.HCl
Molecular Weight: 460.95
Percent Composition: C 62.54%, H 6.34%, N 6.08%, O 17.35%, Cl 7.69%
Properties: Crystals from 3-pentanone + methanol (10:1), mp 188-190°. [a]D -141.0° (c = 0.9 in ethanol). Sol in water, ethanol, methanol.
Melting point: mp 188-190°
Optical Rotation: [a]D -141.0° (c = 0.9 in ethanol)
Derivative Type: Diacid
CAS Registry Number: 86541-78-8
Synonyms: Benazeprilat
Manufacturers' Codes: CGS-14831
Molecular Formula: C22H24N2O5
Molecular Weight: 396.44
Percent Composition: C 66.65%, H 6.10%, N 7.07%, O 20.18%
Properties: mp 270-272°. [a]D -200.5° (c = 1 in 3% aqueous NH4OH).
Melting point: mp 270-272°
Optical Rotation: [a]D -200.5° (c = 1 in 3% aqueous NH4OH)
Therap-Cat: Antihypertensive.
Therap-Cat-Vet: In treatment of congestive heart failure in dogs.
Keywords: ACE-Inhibitor; Antihypertensive; N-Carboxyalkyl (peptide/lactam) Derivatives.