Primary Photoproduct of 2,6-Dimethyl-4-Aminopyrimidine
Primary Photoproduct of 2,6-Dimethyl-4-Aminopyrimidine
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2,6-二甲基-4-氨基嘧啶的初级光产物
DOI:
10.1021/ja00889a048
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发表时间:
1963
期刊:
影响因子:
--
通讯作者:
A. R. Katritsky
中科院分区:
文献类型:
--
作者:
K. Wierzchowski;D. Shugar;A. R. Katritsky
Camphoric anhydride was treated with N-benzyloxyamine according to the method of Ames and Grey3 to form N-benzylcamphorimide (III), mp 80-81; M23d+ 19.2 (CHCU).(Anal. Caled, for C17H2iN03: C, 71.06; H, 7.37; N, 4.87. Found C, 70.99; H, 7.38; N, 4.97.) Hydrogenolysis of IIIgave the N-hy-droxyimide (I) in 51% yield, mp 229-230,[a] 23o+ 7.29 (Anal. Caled, for Ci0H, 5NO3: C, 60.89; H, 7.67; N, 7.10. Found: C, 60.60; H, 7.65; N, 7.20). Absorption in the infrared spectrum characteristic of the N-hydroxyimide group3 occurred at 3.0, 5.74, and 5.95 µ.The rearrangement of 3-nitrocamphor with concen-trated hydrochloric acid gave N-hydroxycamphorimide in 94% yield, mp 229-230;[a] 23d+ 7.46 (CHC13).(Anal. Found: C, 60.76; H, 7.58; N, 7.18.) The infrared spectra of the N-hydroxyimides formedby re-arrangement and by synthesis were identical. The unusual course of the Nef reaction, in contrast to the normal Nef reaction, must be effected by protonation of the carbonylgroup in 3-nitrocamphor to facili-tate the cleavage of the CC bond and the migration of the carbonyl carbon atom with the electrons to form the CN bond which occurs concertedly with the acid catalyzed dehydration of the nitronic acid. Loss of a proton forms the carbonyl group. Protonation and