Bischler–Napieralski reaction

The Bischler–Napieralski reaction is an intramolecular electrophilic aromatic substitution reaction that allows for the cyclization of β-arylethylamides or β-arylethylcarbamates. It was first discovered in 1893 by August Bischler and Bernard Napieralski [de], in affiliation with Basel Chemical Works and the University of Zurich. The reaction is most notably used in the synthesis of dihydroisoquinolines, which can be subsequently oxidized to isoquinolines.

Two types of mechanisms have appeared in the literature for the Bischler–Napieralski reaction. Mechanism I involves a dichlorophosphoryl imine-ester intermediate, while Mechanism II involves a nitrilium ion intermediate (both shown in brackets). This mechanistic variance stems from the ambiguity over the timing for the elimination of the carbonyl oxygen in the starting amide.

In Mechanism I, the elimination occurs with imine formation after cyclization; while in Mechanism II, the elimination yields the nitrilium intermediate prior to cyclization. Currently, it is believed that reaction conditions affect the prevalence of one mechanism over the other (see reaction conditions).

In certain literature, Mechanism II is augmented with the formation of an imidoyl chloride intermediate produced by the substitution of chloride for the Lewis acid group just prior to the nitrilium ion. Because the dihydroisoquinoline nitrogen is basic, neutralization is necessary to obtain the deprotonated product.

The Bischler–Napieralski reaction is carried out in refluxing acidic conditions and requires a dehydrating agent. Phosphoryl chloride (POCl₃) is widely used and cited for this purpose. Additionally, SnCl₄ and BF₃ etherate have been used with phenethylamides, while Tf₂O and polyphosphoric acid (PPA) have been used with phenethylcarbamates. For reactants lacking electron-donating groups on the benzene ring, phosphorus pentoxide (P₂O₅) in refluxing POCl₃ is most effective. Depending on the dehydrating reagent used, the reaction temperature varies from room temperature to 100 °C.

Several reactions that are related to the Bischler–Napieralski reaction are known. In the Morgan–Walls reaction, the linker between the aromatic ring and the amide nitrogen is an ortho-substituted aromatic ring. This N-acyl 2-aminobiphenyl cyclizes to form a phenanthridine. The Pictet–Spengler reaction proceeds from a β-arylamine via condensation with an aldehyde. These two components form an imine, which then cyclizes to form a tetrahydroisoquinoline.

The Pictet–Gams reaction proceeds from an β-hydroxy-β-phenethylamide. It involves an additional dehydration under the same conditions as the cyclization, giving an isoquinoline.^[1][2] As with the Bischler–Napieralski reaction, the Pictet–Gams reaction requires a strongly dehydrating Lewis acid, such as phosphoryl chloride or phosphorus pentoxide.

There are documented variations on the Bischler–Napieralski reaction whose products differ in virtue of either the structure of the initial reactant, the tailoring of reaction conditions, or both. For example, research done by Doi and colleagues suggests that the presence or absence of electron-donating groups on the aryl portion of β-arylethylamides and the ratio of dehydrating reagents influence the patterns of ring closure via electrophilic aromatic substitution, leading to two possible products (see below). Other research on the variations on the Bischler-Napieralski Reaction have investigated the effects of nitro and acetal aryl groups on product formation (see references).

• Pomeranz–Fritsch reaction

• August Bischler, Bernard Napieralski (1893). "Zur Kenntniss einer neuen Isochinolinsynthese". Berichte der Deutschen Chemischen Gesellschaft. 26 (2): 1903–1908. doi:10.1002/cber.189302602143.
• Capilla, A. S.; Romero, M.; Pujol, M. D.; Caignard, D. H.; Renard, P. (2001). "Synthesis of isoquinolines and tetrahydroisoquinolines as potential antitumour agents". Tetrahedron. 57 (39): 8297. doi:10.1016/S0040-4020(01)00826-2.
• Doi, S.; Shirai, N.; Sato, Y. (1997). "Abnormal products in the Bischler–Napieralski isoquinoline synthesis". J. Chem. Soc., Perkin Trans. 1 (15): 2217. doi:10.1039/a701332i.
• Fodor, G. & Nagubandi, S. (1980). "Correlation of the von Braun, Ritter, Bischler-Napieralski, Beckmann and Schmidt reactions via nitrilium salt intermediates". Tetrahedron. 36 (10): 1279. doi:10.1016/0040-4020(80)85039-3.
• Ishikawa, T.; Shimooka, K.; Narioka, T.; Noguchi, S.; Saito, T.; Ishikawa, A.; Yamazaki, E.; Harayama, T.; Seki, H.; Yamaguchi, K. J. (2000). "Anomalous Substituent Effects in the Bischler−Napieralski Reaction of 2-Aryl Aromatic Formamides". Org. Chem. 65 (26): 9143–9151. doi:10.1021/jo0012849. PMID 11149862.
• Wang, X.-j.; Tan, J.; Grozinger, K. (1998). "A significantly improved condition for cyclization of phenethylcarbamates to N-alkylated 3,4-dihydroisoquinolones". Tetrahedron Lett. 39 (37): 6609. doi:10.1016/S0040-4039(98)01395-1.
• Kitson, S. L. (2007). "Mechanism of the Bischler–Napieralski exocyclic and endocyclic dehydration products in the radiosynthesis of (R)-(−)-[6a-¹⁴C]apomorphine". Journal of Labelled Compounds and Radiopharmaceuticals. 50 (5–6): 290. doi:10.1002/jlcr.1270.
• Lee, Jie J. (2007). Name Reactions: A Collection of Detailed Mechanisms and Synthetic Applications. Berlin, Heidelberg: Springer. doi:10.1007/978-3-642-01053-8. ISBN 978-3-642-01053-8.