Downstream synthetic route of 126811-29-8

As the paragraph descriping shows that 126811-29-8 is playing an increasingly important role.

126811-29-8, 7-Bromo-4-chloro-1H-indole is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

7-Amino-3,4-dichloro-1H-indole 7-Bromo-4-chloro-1H-indole obtained from 2-bromo-5-chloronitrobenzene in the same manner as in Production Example 1a was first chlorinated in the same manner as in Production Example 3a, and then the bromo group was converted into an amino group, to give the title compound. 1H-NMR(DMSO-d6) delta (ppm): 5.26(2H, s), 6.29(1H, d, J=8.1 Hz), 6.74(1H, d, J=8.1 Hz), 7.45-7.51(1H, m), 11.08-11.27(1H, m), 126811-29-8

As the paragraph descriping shows that 126811-29-8 is playing an increasingly important role.

Reference£º
Patent; Wakabayashi, Toshiaki; Funahashi, Yasuhiro; Hata, Naoko; Semba, Taro; Yamamoto, Yuji; Haneda, Toru; Owa, Takashi; Tsuruoka, Akihiko; Kamata, Junichi; Okabe, Tadashi; Takahashi, Keiko; Nara, Kazumasa; Hamaoka, Shinichi; Ueda, Norihiro; US2004/18192; (2004); A1;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles