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ChemicalBook--->CAS DataBase List--->4880-92-6

4880-92-6

4880-92-6 Structure

4880-92-6 Structure
IdentificationBack Directory
[Name]

apovincamine
[CAS]

4880-92-6
[Synonyms]

apovincamine
Apovincamina
Apovincaminum
Vinpocetine-2
Unii-504R182zx7
cis-ApovincaMine
Einecs 225-491-0
(+)-trans-Cavinton
Apovincaminum [latin]
Apovincamina [spanish]
Vincamine EP Impurity B
Vinpocetine IMp. B (EP)
Vinpocetine EP Impurity B
Apovincaminic acid methyl
Apo-14,15-dehydrovincamine
Vinpocetine impurity B CRS
(41S,13aS)-methyl 13a-ethyl-
Vinpocetine Related CoMpound B
Methyl (13aS,13bS)-13a-Ethyl-2,3,5,
Methyl (3alpha,16alpha)-eburnamenine-14-carboxylate
(3α,16α)-Eburnamenine-14-carboxylic acid methyl ester
Eburnamenine-14-carboxylic acid, methyl ester, (3α,16α)-
Eburnamenine-14-carboxylic acid, methyl ester, (3-alpha,16-alpha)-
methyl (41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]phthyridine-12-carboxylate
methyl (41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate
Methyl (13aS,13bS)-13a-ethyl-2,3,5,6,13a,13b-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate
Methyl (13as,13bs)-13A-ethyl-2,3,4,6,13A,14B-hexahydro-1H-indilol(3.2.1-de)pyrido(3,2,1-ij)(1,5)naphthylridin-12-carboxylat
IMp. B (EP): Methyl (13aS,13bS)-13a-Ethyl-2,3,5,6,13a,13b-hexahydro-1H-indolo[3,2,1- de]pyrido[3,2,1-ij][1,5]naphthyridine-12- carboxylate (ApovincaMine)
Vinpocetine Related Compound B (30 mg) (methyl (13aS,13bS)-13a-ethyl-9-methoxy-2,3,5,6,13a,13b-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate)
[EINECS(EC#)]

225-491-0
[Molecular Formula]

C21H24N2O2
[MDL Number]

MFCD00867558
[MOL File]

4880-92-6.mol
[Molecular Weight]

336.43
Chemical PropertiesBack Directory
[Melting point ]

160-162℃
[storage temp. ]

Refrigerator
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

neat
[color ]

Off-White to Pale Grey
Safety DataBack Directory
[HS Code ]

2939800000
Hazard InformationBack Directory
[Originator]

Apovincamine,GC Promochem
[Uses]

cis-Apovincamine (Vinpocetine USP Related Compound B), is a vinca alkaloid and a chemical precursor of Vinpocetine (V332500), a derivative of Vincamine with vasodilating activity. Vasodilator (cerebral).
[Definition]

ChEBI: Apovincamine is an alkaloid.
[Manufacturing Process]

Apovincamine is semisynthethetic derivative of (+)-vincamine. Vincamine is alkaloid of Vinca minor. Alcoloid of Tabernaemontana rigida (Apocynaceae) also is used as raw material for preparing of apovincamine. (+)- Vincamine was transformed into oxime ester by reaction with NaNO2 in acetic acid at 0°C -(+/-)-methyl-3-((12bR)-1-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3- a]quinolizin-1-yl)-2-(hydroxyimino)propanoate, which was resolved on the isomers with dibenzoyl D-tartratic acid. (-)-Methyl 3-((12bR)-1-ethyl- 1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-1-yl)-2- (hydroxyimino)propanoate was re-crystallized from methanol to afford (-)- methyloxime ester, MP: 195°C.
2 g of above oxime methyl ester was heated in mixture of methanol (37.5 ml) and conc. H2SO4 (13.5 ml) on water bath for 1 hour. The solution was poured into ice-water (80 ml), basified with conc. NH4OH to pH 9, and extracted with CH2Cl2 (3x20 ml). The combined extracts were dried (MgSO4), filtered, evaporated in vacuum and the residue was re-crystallized from MeOH (5 ml) to yield 1.32 g (72.5%) of (+)-apovincamine, MP: 160°-162°C.
[Therapeutic Function]

Vasodilator
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