Synthesis of polyfunctional secondary amines by the addition of functionalized zinc reagents to nitrosoarenes †

Addition of functionalized aryl, heteroaryl or adamantyl zinc reagents to various nitroso-arenes in the presence of magnesium salts and LiCl in THFproducesafter areductivework-upwithFeCl 2 andNaBH 4 inethanol the corresponding polyfunctional secondary amines in high yields.

Synthesis of polyfunctional secondary amines by the addition of functionalized zinc reagents to nitrosoarenes † Vasudevan Dhayalan, Christoph Sämann and Paul Knochel* Addition of functionalized aryl, heteroaryl or adamantyl zinc reagents to various nitroso-arenes in the presence of magnesium salts and LiCl in THF produces after a reductive work-up with FeCl 2 and NaBH 4 in ethanol the corresponding polyfunctional secondary amines in high yields.
The preparation of arylamines is an important synthetic goal since these compounds often have useful properties for pharmaceuticals or material science applications. 1 Transition metal catalyzed aminations have been well studied, 2 but the use of expensive and toxic metallic catalysts reduces somewhat the utility of such synthetic methods. Another approach has been the use of electrophilic nitrogen reagents and their reactions with non-expensive and low toxic main-group organometallics. 3 A few years ago, we have reported that functionalized arylmagnesium reagents add to nitroso-arenes 4 and nitro-arenes. 5 Although satisfactory yields were obtained, the high reactivity of the carbon-magnesium bond reduces the functional group tolerance. Furthermore, nitroso-arenes have proven to be versatile reagents for performing nitroso aldol and related reactions. 6 Herein, we wish to report a mild synthesis of diaryl or heteroaryl-(aryl)amines as well as functionalized highly sterically hindered adamantyl(aryl)amines. Thus, the treatment of an arylzinc derivative 2, prepared either by the direct insertion of Mg in the presence of LiCl and ZnCl 2 (ref. 7) or by a I/Mg-exchange with iPrMgClÁLiCl 8 followed by transmetalation with ZnCl 2 , with various nitroso-arenes of type 3 9 affords an intermediate zincated hydroxylamine derivative 4 which after reductive work-up with FeCl 2 and NaBH 4 in ethanol (25 1C, 15 h) produce the corresponding secondary amines of type 5 in excellent yields (Scheme 1). A range of functional groups have been tolerated in the starting arylzinc reagent as shown in Table 1.
Thus, PhZnCl (1.1 equiv.) prepared by the direct insertion of Mg in the presence of LiCl and ZnCl 2 reacts with nitrosobenzene 3a (1.0 equiv.) at 25 1C within 2-3 h and produces after reductive work-up with FeCl 2 (2.0 equiv.) and NaBH 4 (1.0 equiv.) in ethanol (25 1C, 15 h) the corresponding diphenylamine 5a in 85% yield (Table 1, entry 1). 10a The presence of both Mg salts and LiCl were found to be essential for achieving a high yield. A variety of arylzinc reagents prepared similarly were used in the addition to 3a. Both electron withdrawing and donating groups can be attached at the aryl ring (Table 1, entries 2-8). 10b-g Arylzinc reagent 2c has been prepared via an I/Mg-exchange, 8 its reaction with nitrosobenzene (3a) furnishes the corresponding secondary amine 5c in 76% yield (Table 1, entry 3). Although sensitive functional groups like a formyl or an acetyl group are not tolerated, the corresponding bromoacetal (1i) or bromoketal (1j) are readily converted to the zinc reagents (2i and 2j) by the insertion of Mg in the presence of LiCl and ZnCl 2 . 7 The addition of nitrosobenzene (3a) provides after removal of the ethylene glycol protecting group (CF 3 CO 2 H in CH 2 Cl 2 at 25 1C for 5-8 h) the secondary amines (5i and 5j) in 64-75% yield (Table 1, entries 9 and 10).
This addition reaction can be extended to various nitroso-arenes (commercially available) or prepared according to the method of Bäckvall. 11 Again, electron-donating or accepting substituents are tolerated in the arylnitroso reagents of type 3 furnishing the Scheme 1 Synthesis of polyfunctional secondary amines of type 5 via the addition of functionalized zinc reagents of type 2 to various nitroso compounds of type 3.
The research leading to these results has received funding from the European Research Council under the European Community's Seventh Framework Programme (FP7/2007-2014) ERC grant agreement no. 227763. We thank the Fonds der Chemischen Industrie for financial support. We also thank Heraeus Holding GmbH (Hanau), Rockwood Lithium (Frankfurt), and BASF SE (Ludwigshafen) for the generous gift of chemicals. a General reaction conditions: arylzinc reagent (1.1 equiv.), nitroso electrophile (1.0 equiv.), NaBH 4 (1.0 equiv.), FeCl 2 (2.0 equiv.). b Yield of analytically pure isolated product as determined by 1 H-NMR analysis. c Prepared by I/Mg-exchange with iPrMgClÁLiCl. 8 d The TMS-group was cleaved during workup and column chromatography purification. e The arylzinc reagents (2i and 2j) were prepared from the corresponding bromides (see ESI). f Obtained after removal of the ethylene glycol group with CF 3 CO 2 H in CH 2 Cl 2 (see ESI).    (56) a General reaction conditions: alkylzinc reagent (1.1 equiv.), nitroso electrophile (1.0 equiv.), NaBH 4 (1.0 equiv.), FeCl 2 (2.0 equiv.). b Yield of analytically pure isolated product as determined by 1 H-NMR analysis. c Prepared by transmetalation of commercially available t-BuMgCl with ZnCl 2 .