You are using Science Of Synthesis as a Guest.
Please login to access the full content or check if you have access via16.12.1.3.2.1 Reaction of Aryl Methyl Ketones with Aryl Aldehydes, Aryl Cyanides, and Hydroxylamine
Please login to access the full content or check if you have access via
von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 117.
Aryl methyl ketones, aromatic aldehydes, aromatic nitriles, and hydroxylamine undergo a one-pot, four-component reaction under solvent-free conditions and microwave irradiation to produce 2,4,6-triarylpyrimidines 59 (Scheme 24).[69] The reported yields are in the range of 86 to 95%. It is assumed that two distinct reactions occur prior to the ring closure: formation of a chalcone and formation of an amidoxime. These and similar components are often used in pyrimidine synthesis (see Section 16.12.1.7.4.21).
Meeeee 88 8,8,8-Meeeeeeeeeeeeeeeee eeee Meee Meeeee Meeeeee, Meee Meeeeeeee, Meee Meeeeeee, eee Meeeeeeeeeeee[88]
Me8 | Me8 | Me8 | Meeee (%) | Mee |
---|---|---|---|---|
Me | Me | Me | 88 | [88] |
Me | Me | 8-MeMM8M8 | 88 | [88] |
Me | 8-M8MM8M8 | Me | 88 | [88] |
8-eeeeeeee | Me | Me | 88 | [88] |
Meeeeeeeeeee Meeeeeeee
8,8,8-Meeeeeeeeeeeeeeeeee (88, Me8 = Me8 = Me8 = Me); Meeeeee Meeeeeeee:[88]
M eeeeeee ee eeeeeeeeeeee (8.88 e, 8 eeee), MeMMM (8.88 e, 8 eeee), eee eeeeeeee MeMM (8.88 e, 8.88 eeee) eee eeeeeee ee 88°M eee 8.8 e. Meeee e eeeeee eeeeeeeeeeee eeeeeeeeee eeee eee eeeeeeeeeeeee eeeeeeee, ee eeeeeeeee ee MMM eeeeeeeeee, eeeeeeeeeeee (8.88 e, 8.8 eeee), 88% MM8MM (8.88 e, 8.8 eeee), eee MeMM (e eeeeeeeee eeeeee, eee eeeeeee eeee 8.88 eeee) eeee eeeee ee eee eeeeeee eee eeeeeeee eee eeeeeeeee ee 88°M eee e eeeeeee 8.8 e. Mee eeeeeee eee eeee eeeeeeeeee ee e eeeeeeeee eeee ee 888°M eee 8 eee. Meeeeee eeeeee eee eeeeeeeeeeee ee eeeeee eeeeeeeeeeeeee (eeeeee eee, eeeeee/MeMMe 8:8) eeeeeeee eee eeeeeee; eeeee: 88%; ee 888–888°M.
References
[69] | Meee, M.; Meeeeeee, M.; Meeeeee, M.; Meeeeeeeee, M. M., Meeeeeeeeee Meee., (8888) 88, 8888. |