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CONIVAPTAN

CAS No.
210101-16-9
Chemical Name:
CONIVAPTAN
Synonyms
CONIVAPTAN;Kaunivartan;ZINC 12503187;N-[4-(2-methyl-4,5-dihydro-3H-imidazo[4,5-d][1]benzazepine-6-carbonyl)phenyl]-2-phenylbenzamide;N-[4-[(4,5-Dihydro-2-methylimidazo[4,5-d][1]benzazepin-6(1H)-yl)carbonyl]phenyl]-[1,1'-biphenyl]-2-carboxamide;[1,1'-Biphenyl]-2-carboxamide, N-[4-[(4,5-dihydro-2-methylimidazo[4,5-d][1]benzazepin-6(1H)-yl)carbonyl]phenyl]-
CBNumber:
CB51011161
Molecular Formula:
C32H26N4O2
Molecular Weight:
498.583
MDL Number:
MFCD09838361
MOL File:
210101-16-9.mol
MSDS File:
SDS
Last updated:2023-05-15 10:43:30

CONIVAPTAN Properties

FDA UNII 0NJ98Y462X
ATC code C03XA02

CONIVAPTAN price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth Carbosynth FC159956 Conivaptan 210101-16-9 10mg $70 2021-12-16 Buy
Biosynth Carbosynth FC159956 Conivaptan 210101-16-9 25mg $125 2021-12-16 Buy
Biosynth Carbosynth FC159956 Conivaptan 210101-16-9 50mg $200 2021-12-16 Buy
Biosynth Carbosynth FC159956 Conivaptan 210101-16-9 100mg $300 2021-12-16 Buy
Biosynth Carbosynth FC159956 Conivaptan 210101-16-9 250mg $400 2021-12-16 Buy
Product number Packaging Price Buy
FC159956 10mg $70 Buy
FC159956 25mg $125 Buy
FC159956 50mg $200 Buy
FC159956 100mg $300 Buy
FC159956 250mg $400 Buy

CONIVAPTAN Chemical Properties,Uses,Production

Description

Conivaptan, a vasopressin antagonist, was discovered and developed by Yamanouchi for the treatment of hyponatraeum associated with congestive heart failure.

Uses

2-Methyl-1,4,5,6-tetrahydrobenzo[b]imidazo[4,5-d]azepine is an impurity of Conivaptan(C384700). Conivaptan is used in the treatment of congestive heart failures.

Definition

ChEBI: The amide resulting from the formal condensation of 4-[(biphenyl-2-ylcarbonyl)amino]benzoic acid with the benzazepine nitrogen of 2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine. It is an antagonist for two of the three types of argini e vasopressin (AVP) receptors, V1a and V2. It is used as its hydrochloride salt for the treatment of hyponatraemia (low blood sodium levels) caused by syndrome of inappropriate antidiuretic hormone (SIADH).

Synthesis

After looking at several different approaches to the synthesis, a convergent approach, shown in the Scheme 4, was developed for large scale synthesis. Bromination of benzazepinone 10 with pyridinium hydrobromide perbromide in chloroform followed by recrystallization gave bromide 11. Reaction of bromide 11 with ethaneimidate hydrochloride in the presence of potassium carbonate in toluene or chloroform gave the desired imidazole 12 in 69% yield. Although chlo-roform provided a slightly better yield, for large scale preparation, toluene was used to minimize halogenated solvent waste and because the quality of product was similar or better than with use of chloroform. Deprotection of the tosylate was found to be effective with heating the sulfonamide 12 in 80% sulfuric acid at 80oC. The benzazepinone product 13 was obtained in 90% yield after crystallization from acetonitrile and water mixture.
Synthesis of the coupling partner 16 required to provide conivaptan was synthesized in 95% yield from biphenyl 2- benzoic acid via sequential reaction with thionyl chloride in toluene followed by coupling with aminobenzoic acid in acetone with N,N-dimethylaniline as a base. High quality acid 16 was obtained by crystallization from DMF and water. The acid 16 was activated by converting it into acid chloride with thionyl chloride in acenonitrile, to which was added imidazo benzazepine 13 in toluene and, after recrystallization in acidic ethanol, gave conivaptan hydrochloride (III) in 90% yield.

Synthesis_210101-16-9

CONIVAPTAN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 39)Suppliers
Supplier Tel Email Country ProdList Advantage
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 965 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28172 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29811 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32165 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118 xie@china-sinoway.com China 988 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8467 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43340 58
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd
+86-18791163155 +86-13119157289 13119157289@163.com China 2973 58
Wuhan Jingkang en Biomedical Technology Co., Ltd
+8613720134139 orders@jknbiochem.com China 5221 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131957 58

View Lastest Price from CONIVAPTAN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
CONIVAPTAN pictures 2019-12-26 CONIVAPTAN
210101-16-9
US $1.00 / g 1g ≥98% g/kg/Ton Career Henan Chemical Co
  • CONIVAPTAN pictures
  • CONIVAPTAN
    210101-16-9
  • US $1.00 / g
  • ≥98%
  • Career Henan Chemical Co
CONIVAPTAN N-[4-[(4,5-Dihydro-2-methylimidazo[4,5-d][1]benzazepin-6(1H)-yl)carbonyl]phenyl]-[1,1'-biphenyl]-2-carboxamide N-[4-(2-methyl-4,5-dihydro-3H-imidazo[4,5-d][1]benzazepine-6-carbonyl)phenyl]-2-phenylbenzamide ZINC 12503187 [1,1'-Biphenyl]-2-carboxamide, N-[4-[(4,5-dihydro-2-methylimidazo[4,5-d][1]benzazepin-6(1H)-yl)carbonyl]phenyl]- Kaunivartan 210101-16-9 API