New learning discoveries about 19012-02-3

The synthetic route of 19012-02-3 has been constantly updated, and we look forward to future research findings.

19012-02-3, 3-Acetyl-1-methylindole is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

EXAMPLE 17 N-hydroxy-N-(1-(1-methylindol-3-yl)ethyl) urea The desired compound was prepared using the method of example 2, except using 1-methyl-3-acetyl indole, prepared as described in example 16, step a instead of acetyl benzo[b]thiophene. (R1 =NH2, A=CHCH3, X=NCH3 [3-isomer], Y=H). Melting Point: 149-150 C. NMR (300 MHz, DMSO-d6): 1.46 (d, 3H, J=7.5 Hz); 3.74 (s, 3H); 5.66 (q, 1H); 6.18 (br s, 2H); 6.94-7.15 (m, 2H); 7.24 (s, 1H); 7.36 (m, 1H); 7.64 (m, 1H); 8.88 (s, 1H). Mass Spectrum (CI-NH3): 234 (M+H)+, 251 (M+NH4)+, 158., 19012-02-3

The synthetic route of 19012-02-3 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Abbott Laboratories; US4873259; (1989); A;,
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