Novel synthesis of 1,2,3,4-tetrahydropyrazino[1,2-a]indoles

37Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free