| | Identification | Back Directory |  | [Name] 
 MAGNOLINE
 |  | [CAS] 
 6859-66-1
 |  | [Synonyms] 
 MAGNOLINE
 (1R)-1,2,3,4-Tetrahydro-1-[[4-[2-hydroxy-5-[[(1S)-1,2,3,4-tetrahydro-7-hydroxy-6-methoxy-2-methylisoquinolin-1-yl]methyl]phenoxy]phenyl]methyl]-6-methoxy-2-methylisoquinolin-7-ol
 7-Isoquinolinol, 1,2,3,4-tetrahydro-1-[[4-[2-hydroxy-5-[[(1S)-1,2,3,4-tetrahydro-7-hydroxy-6-methoxy-2-methyl-1-isoquinolinyl]methyl]phenoxy]phenyl]methyl]-6-methoxy-2-methyl-, (1R)-
 |  | [Molecular Formula] 
 C36H40N2O6
 |  | [MDL Number] 
 MFCD07781417
 |  | [MOL File] 
 6859-66-1.mol
 |  | [Molecular Weight] 
 596.71
 | 
 | Chemical Properties | Back Directory |  | [Melting point ] 
 178-179°
 |  | [alpha ] 
 D -9.6° (pyridine)
 |  | [Boiling point ] 
 738.3±60.0 °C(Predicted)
 |  | [density ] 
 1.254±0.06 g/cm3(Predicted)
 |  | [pka] 
 9.31±0.45(Predicted)
 | 
 | Hazard Information | Back Directory |  | [Description] 
 A closely-related bisbenzylisoquinoline base found also in Magnolia fuscata, the 
alkaloid occurs mainly in the leaves and is obtained in the pure form as a microcrystalline powder from EtOH or C6H6. It may be separated from magnolamine 
by virtue of its insolubility in hot C6H6. It is only sparingly soluble in most 
organic solvents but dissolves readily in aqueous alkalies. The alkaloid is laevorotatory with [α]D - 9.6° (pyridine). It furnishes vitreous salts with mineral 
acids but yields a crystalline picrate as a yellow microcrystalline powder from 
EtOH, m.p. 160-2°C (dec.) and a picrolonate, m.p. 190°C (dec.). Treatment 
with CH2N2 gives the trimethyl ether, m.p. 1 09-1 10°C, oxidized by KMn04 in 
Me2CO to 2-methoxy-5:4'-dicarboxydiphenyl ether and a lactam, l-keto-6:7-
dimethoxy-2-methyltetrahydroisoquinoline. On the basis of these results, the 
alkaloid may be represented by the above structure which makes it a close 
relative of dauricine (q.v.). The Ullmann reaction has been used by Kametani 
and his colleagues to synthesize the alkaloid.
 |  | [Definition] 
 ChEBI: Berbamunine is a benzyltetrahydroisoquinoline, a bisbenzylisoquinoline alkaloid and an isoquinolinol. It is a conjugate base of a berbamuninium(2+).
 |  | [References] 
 Pyman., J. Chern. Soc., 95, 1272 (1909) 
Proskurnina, Orekhov., Bull. Soc. Chirn., 5, 1357 (1958) 
Proskurnina, Orekhov., J. Gen. Chern. USSR., 10, 707 (1940) 
Synthesis: 
Kametani, !ida, Sakurai., Chern. Pharrn. Bull. (Tokyo), 16, 1623 (1968)
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