Synthesis 2004(8): 1183-1186  
DOI: 10.1055/s-2004-822351
PAPER
© Georg Thieme Verlag Stuttgart · New York

New Synthesis of 3-Substituted Indazoles from 3-Trimethylsilylindazole

Yoshiyuki Hari, Yoshimichi Shoji, Toyohiko Aoyama*
Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya 467-8603, Japan
Fax: +81(52)8363439; e-Mail: aoyama@phar.nagoya-cu.ac.jp;
Further Information

Publication History

Received 17 February 2004
Publication Date:
28 April 2004 (online)

Abstract

Reaction of aryl aldehydes with 3-trimethylsilylindazole in the presence of CsF easily gave the corresponding 3-(arylhydroxymethyl)indazoles in good to moderate yields.

8

No reaction occurred at r. t.

9

In fact, in the reaction of 3-trimethylsilylindazole(1) with PhCHO, the use of K2CO3 in place of CsF as a base gave the desired product 5a (58 %) together with indazole(4) (37 %). Reaction conditions: PhCHO (10 equiv), K2CO3 (1.5 equiv), MS 3Å, DMF, 80 °C, 6 h.

10

Probably, the Brook rearrangement giving the irreversible O-silyl intermediate 8 would accelerate this reaction.