Abstract
Condensation of 2-(3-methyl-1H-indol-1-yl)ethylamine (7) with benzotriazole and formaldehyde gave 2-(1H- 1,2,3-benzotriazol-1-ylmethyl)-10-methyl-1,2,3,4-tetrahydro- pyrazino[1,2-a]indole (8) in 96% yield. Nucleophilic substitutions of the benzotriazolyl group in 8 with NaBH4, NaCN, triethyl phosphite, allylsilanes, silyl enol ether and Grignard reagents afforded novel 10-methyl-1,2,3,4-tetrahydropyrazino- [1,2-a]indoles 9a-i in 78-95% yields.
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CITATION STYLE
Katritzky, A. R., Verma, A. K., He, H. Y., & Chandra, R. (2003). Novel synthesis of 1,2,3,4-tetrahydropyrazino[1,2-a]indoles. Journal of Organic Chemistry, 68(12), 4938–4940. https://doi.org/10.1021/jo026922x
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