Functionalization of 1H-Pyrrolo (2, 3-b) pyridine.

S Minakata, S Itoh, M Komatsu, Y Ohshiro

Index: Minakata, Satoshi; Itoh, Shinobu; Komatsu, Mitsuo; Ohshiro, Yoshiki Bulletin of the Chemical Society of Japan, 1992 , vol. 65, # 11 p. 2992 - 2997

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Citation Number: 15

Abstract

Functionalization of 1H-pyrrolo [2, 3-b] pyridine (7-azaindole) was studied to provide new compounds directing toward agrochemicals and/or functional materials. Amino groups such as NH 2, NH (CH 2) 2 NH 2, and NH (CH 2) 2 NH (CH 2) 2 NH 2 were introduced onto 6- position of 7-azaindole to form multidentate agents. 6-Amino and 6-iodo derivatives were easily converted to podant-type compounds, N, N′-bis (1H-pyrrolo [2, 3-b] pyridin-6-yl)-1, ...