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. Author manuscript; available in PMC: 2015 Dec 15.
Published in final edited form as: Angew Chem Int Ed Engl. 2014 Oct 21;53(51):14191–14195. doi: 10.1002/anie.201408335

Table 2.

Substrate Scope for the Rh(II)-Catalyzed Reaction of Pyridotriazoles with Anilines and Aliphatic Amines.[a,b]

graphic file with name nihms635251t42.jpg

Entry Product Yield,
%
Entry Product Yield,
%
1 graphic file with name nihms635251t43.jpg 88 7 graphic file with name nihms635251t44.jpg 71
2 graphic file with name nihms635251t45.jpg 63 8 graphic file with name nihms635251t46.jpg 90
3 graphic file with name nihms635251t47.jpg 80 9 graphic file with name nihms635251t48.jpg 47
4 graphic file with name nihms635251t49.jpg 86 10 graphic file with name nihms635251t50.jpg 91[c]
5 graphic file with name nihms635251t51.jpg 72 11 graphic file with name nihms635251t52.jpg 87
6 graphic file with name nihms635251t53.jpg 76 12 graphic file with name nihms635251t54.jpg 82
[a]

Conditions: triazole 1 (0.20 mmol), N–H compounds 2 (1.5 equiv.), and Rh2(esp)2 (3.0 mol %) were heated in 2 ml of dry DCE at 120 °C until completion.

[b]

Isolated yields.

[c]

1.0 mol % of Rh2(esp)2.