| Identification | Back Directory | [Name]
Dimemorfan phosphate | [CAS]
36304-84-4 | [Synonyms]
Hofvan
Astomin
Dimemomin
DIMEMORFAN PHOSPHATE
dimemorphan phosphate
Dimemorfan phosphate USP/EP/BP
Morphinan, 3,17-dimethyl-, (9α,13α,14α)-, phosphate (1:1)
(9alpha,13alpha,14alpha)-3,17-dimethylmorphinan dihydrogen phosphate | [EINECS(EC#)]
252-958-6 | [Molecular Formula]
C18H25N.H3O4P | [MDL Number]
MFCD01714607 | [MOL File]
36304-84-4.mol | [Molecular Weight]
353.396 |
| Questions And Answer | Back Directory | [Preparation]
Under nitrogen protection, the starting materials 3-methoxy-17-methyldextralan (5.71 g, 20 mmol) and bis(tricyclohexylphosphine) nickel dichloride (0.70 g, 1 mmol) were added to 100 mL of toluene and stirred until dissolved. The mixture was heated to 65 °C, and methyl magnesium bromide (tetrahydrofuran solution) (1 mol/L, 20 mL, 20 mmol) was added dropwise. After the addition was complete, the mixture was kept at this temperature. TLC was used to detect the complete reaction of the starting materials. The mixture was then cooled to room temperature, and a small amount of saturated ammonium chloride solution was added dropwise to quench the reaction. The mixture was washed with water to separate the layers, and the organic layer was separated. The organic layer was washed with saturated brine, dried, and then distilled under reduced pressure to remove toluene, yielding dimethylphenidate. Without purification, 25 mL of 95% ethanol was added and stirred until dissolved at room temperature. Then, 85% phosphoric acid (2.3 g, 20 mmol) was added, and a white solid precipitated. After filtration, washing, and drying, 5.46 g of Dimemorfan phosphate was obtained, with a yield of 77.4% and a purity of 96.2%. |
| Chemical Properties | Back Directory | [Melting point ]
267-269° | [alpha ]
D23 +25.7° (c = 0.5 in methanol) | [storage temp. ]
Store at -20°C | [solubility ]
Water : 20 mg/mL (56.59 mM);DMSO : 1 mg/mL (2.83 mM) | [form ]
Solid | [color ]
White to off-white |
| Safety Data | Back Directory | [Safety Profile]
Poison by intravenous,
intraperitoneal, and subcutaneous routes.
Moderately toxic by ingestion. An
experimental teratogen. Experimental
reproductive effects. Used as an antitussive agent. When heated to decomposition it
emits very toxic fumes of NOx and POx. | [Toxicity]
LD50 in mice (mg/kg): 223 s.c.; 475 orally (Kasé) |
| Hazard Information | Back Directory | [Originator]
Astomin,Yamanouchi
Pharmaceutical Co.,
Ltd. | [Manufacturing Process]
Preparation of 1-p-methylbenzyl-1,2,5,6,7,8-hexahydroisoquinoline:
a) To a suspension of 2.24 g of a metallic magnesium in 36 ml of an 1:1
mixture of tetrahydrofuran and ether was added dropwise a solution of 13.5 g of p-methylbenzyl chloride in 36 ml of an 1:1 mixture of tetrahydrofuran and
ether over a period of about 30 min and then the resultant mixture was
refluxed under heating for 30 min. The solution thus obtained was added
dropwise to a suspension of 17.5 g of 2-methyl-5,6,7,8-tetrahydroisoquinoline
bromide in 90 ml of an 1:1 mixture of tetrahydrofuran and ether cooled to 0-
5°C over a period of about 25 min. After stirring the mixture for 2 hours at
temperatures of from 0-5°C, 100 ml of cooled ether and 1.7 N ammonia were
added to the reaction product liquid and after shaking sufficiently the system,
the ether layer thus formed was recovered. The product in the aqueous layer
was further extracted with 50 ml of ether. The ether extract was combined
with the ether layer recovered above and then the product in the mixture was
extracted 4-times with 30 ml each of 1 N hydrochloric acid cooled. To the
hydrochloric acid extract was added 100 ml of cooled 1.7 N ammonia, and the
oily material formed was extracted thrice with 80 ml each of ether. After
drying the ether extract over anhydrous potassium carbonate, ether was
distilled away to provide 15.4 g of oily 1-p-methylbenzyl-1,2,5,6,7,8-
hexahydroisoquinoline.
b) In a mixture of 300 ml of methanol and 30 ml of water were dissolved 15.4
g of oily 1-p-methylbenzyl-2-methyl-1,2,5,6,7,8-hexahydroisoquinoline and
while stirring the mixture, 2 g of sodium borohydride was added little by little
to the mixture at room temperature over a period of about 15 min. After
stirring the light yellow solution obtained overnight at room temperature, the
solvent was distilled away under a reduced pressure. The residue was mixed
with 50 ml of water and 150 ml of ether and after sufficiently shaking the
mixture, the ether layer formed was separated. The aqueous layer thus
separated was adjusted to basicity by the addition of a small amount of 1.7 N
ammonia and then the product in the layer was extracted with 100 ml of
ether. The ether layer separated above was combined with the ether extract
and after washing the mixture with 1.7 N ammonia and water, the mixture
was dried over anhydrous potassium carbonate and then ether was distilled
away to provide 13.8 g of an orange oily material. By subjecting the product
to a distillation under a reduced pressure, oily D-1-p-methylbenzyl-2-methyl1,2,3,4,5,6,7,8-octahydroisoquinoline was obtained. Boiling point 133-
136°C/0.35 mm Hg.
Preparation of D-3-methyl-N-methylmorphinane:
To 130 ml of 85% phosphoric acid was added 26.5 g of D-1-p-methylbenzyl2-methyl-1,2,3,4,5,6,7,8-octahydroisoquinoline and the mixture was heated to
130-140°C for 72 hours. After the reaction was over, the reaction product
liquid was dispersed in ice-water and the solution was made strongly alkaline
by the addition of about 300 ml of concentrated aqueous ammonia, whereby
an oily material and a crystal were formed. The aqueous solution was mixed
with 500 ml of water and 500 ml of ether followed by sufficient shaking;
thereafter, the aqueous layer and the ether layer were separated. The
aqueous layer was extracted with 500 ml of ether and the extract was
combined with the ether layer separated above. Black resinous material
floating in the mixture was filtered away. After washing with water the ether
solution thus obtained and drying over anhydrous potassium carbonate, 14 g
of a black-orange oily material was obtained. When the oily material was
immediately distilled under a reduced pressure, 11 g of a faint yellow
transparent oily material showing a boiling point of 130-136°C/ 0.3 mm Hg
was obtained. The product was crystallized immediately after distillation. The crystals were recrystallized from 12 ml of acetone, recovered by filtration, and
washed with 7 ml of acetone to provide 7.3 g of the white prism crystal of D3-methyl-N-methylmorphinane. Furthermore, from the filtrate in the
recrystallization were recovered the same crystals. Melting point 90-93°C,
[α]D22 = +51.5° (c=1, methanol).
| [Therapeutic Function]
Antitussive |
|
|