20289-27-4, 7-(Benzyloxy)-1H-indole is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated
EXAMPLE 93 Preparation of 7-Benzyloxy-3-{4-[(1H-2-methylimidazo[4,5-c]pyrid-1-yl)methyl]benzoyl}indole The desired compound was prepared according to the method of Example 90, except substituting 7-benzyloxyindole for 4,7-dimethoxycarbonylindole. 1 H NMR (DMSO-d6, 300 MHz) delta2.59 (s, 3H), 5.30 (s, 2H), 5.63 (s, 2H), 6.93 (d, 1H, J=7.7 Hz), 7.13 (t, 1H, J=7.9 Hz), 7.28 (d, 2H, J=8.1 Hz), 7.32-7.46 (c, 3H), 7.54-7.60 (c, 2H), 7.62 (d, 1H, J=5.1 Hz), 7.71 (d, 1H, J=2.2 Hz), 7.76 (d, 2H), J=8.5 Hz), 7.80 (d, 1H, J=8.1 Hz), 8.30 (d, 1H, J=5.2 Hz), 8.87 (s, 1H), 12.24 (d, 1H, J=2.6 Hz). MS (DCI/NH3) m/e 473 (M+H)+. IR, cm-1 (microscope) 738 (m), 1219 (m), 1248 (m), 1278 (m), 1436 (s). Anal calcd for C30 H24 N4 O2.1.2 H2 O: C, 72.92; H, 5.38; N, 11.34. Found: C, 72.97; H, 5.30; N, 11.05., 20289-27-4
20289-27-4 7-(Benzyloxy)-1H-indole 260798, aindole-building-block compound, is more and more widely used in various fields.
Reference：
Patent; Abbott Laboratories; US5486525; (1996); A;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
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