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Metildigoxin

CAS No.
30685-43-9
Chemical Name:
Metildigoxin
Synonyms
Lanitop;MEDIGOXIN;Metildigoxin;b-Methyldigoxin;Metildigoxin RS;β-Methyl Digoxin;-β-Methyl Digoxin;beta-Methyldigoxin;4'''-Methyldigoxin;4'''-b-Methyldigoxin
CBNumber:
CB7875234
Molecular Formula:
C42H66O14
Molecular Weight:
794.97
MDL Number:
MFCD00869434
MOL File:
30685-43-9.mol
Last updated:2023-05-15 10:43:54

Metildigoxin Properties

Melting point 200-202°C (dec.)
Boiling point 668.38°C (rough estimate)
Density 1.1020 (rough estimate)
refractive index 1.6130 (estimate)
storage temp. Hygroscopic, Refrigerator, Under Inert Atmosphere
solubility DMSO (Sparingly), Methanol (Slightly)
pka 13.50±0.70(Predicted)
form Solid
color White to Off-White
Stability Hygroscopic
FDA UNII I7GG1YUC5V
ATC code C01AA08

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS06
Signal word  Danger
Hazard statements  H412-H319-H330-H300-H372
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501-P260-P264-P270-P314-P501-P273-P501-P264-P270-P301+P310-P321-P330-P405-P501
Toxicity LD50 in rats, mice (mg/kg): 4.8, 4.9 i.v.; 6.2, 4.8 i.p.; 8.3, 7.8 orally (Czerwek)

Metildigoxin Chemical Properties,Uses,Production

Chemical Properties

White Solid

Originator

Lanitop,Boehringer Mannheim,W. Germany,1972

Uses

Cardiotonic. Obtained by the O-methylation of Digoxin.

Definition

ChEBI: Metildigoxin is a cardenolide glycoside.

Manufacturing Process

Digoxin (10 g) is dissolved in a mixture of dimethylformamide (80 ml) and dioxane (80 ml) and then strontium hydroxide (3.5 g) and aluminum oxide (10 g, activity 1-2 according to Brockmann) are added. To this suspension methyl mesylate (9.3 g), dissolved in dioxane (80 ml) is added dropwise within one hour in the presence of an inert gas and under stirring. After the addition of the methylating agent is completed, the reaction mixture is stirred for further 5 hours, then chloroform (160 ml) is added, the precipitate is filtered off, washed with chloroform (100 ml), pyridine (40 ml) is added to the filtrate, which is then concentrated in vacuo to an oily residue. The latter is diluted with chloroform (300 ml) and extracted four times with distilled water (40 ml portions). The combined chloroform extracts are dried with anhydrous sodium sulfate and then concentrated in vacuo to a dry residue. Therefrom βmethyldigoxin is eluted on a SiO2 column with a chloroformlethanol mixture (93:7). After recrystallization from ethyl acetate, saturated with water, the yield of β-methyldigoxin is 6.7 g; MP 225°C to 229°C. IR spectrum is identical with the spectrum of standard methyldigoxin.

Therapeutic Function

Cardiotonic

Metildigoxin Preparation Products And Raw materials

Raw materials

Preparation Products

beta-Methyldigoxin Metildigoxin MEDIGOXIN 4'''-b-Methyldigoxin 4'''-Methyldigoxin 4'''-O-Methyldigoxin b-Methyldigoxin Card-20(22)-enolide, 3-[(O-2,6-dideoxy-4-O-methyl-b-D-ribo-hexopyranosyl-(14)-O-2,6-dideoxy-b-D-ribo-hexopyranosyl-(14)-2,6-dideoxy-b-D-ribo-hexopyranosyl)oxy]-12,14-dihydroxy-, (3b,5b,12b)- (9CI) Digoxin, 4'''-O-methyl- (8CI) Lanitop 3β-[[4-O-[4-O-(4-O-Methyl-2,6-dideoxy-β-D-ribo-hexopyranosyl)-2,6-dideoxy-β-D-ribo-hexopyranosyl]-2,6-dideoxy-β-D-ribo-hexopyranosyl]oxy]-12β,14-dihydroxy-5β,14β-card-20(22)-enolide Metildigoxin RS Card-20(22)-enolide, 3-[(O-2,6-dideoxy-4-O-methyl-β-D-ribo-hexopyranosyl-(1→4)-O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-2,6-dideoxy-β-D-ribo-hexopyranosyl)oxy]-12,14-dihydroxy-, (3β,5β,12β)- Metildigoxin USP/EP/BP β-Methyl Digoxin -β-Methyl Digoxin 30685-43-9 C41H63ClO14 C42H66O14 Carbohydrates & Derivatives Intermediates & Fine Chemicals Pharmaceuticals Steroid