HCID 86651965, compound → HCID 178517047, compound

Participants

Reaction Steps

According to the procedure for the synthesis of (E)-3-((1H-indazol-6-yl)methylene)indolin-2-one, except substituting 3-(thiazol-2-yl)-1H-indazole-6-carbaldehyde (4.6 mg, 0.02 mmol), the title compound was prepared as a yellow solid (2.3 mg, 36%). 1H NMR (400 MHz, d6-DMSO) δ 13.75 (br. s, 1H), 10.64 (br. s, 1H), 8.44 (d, J=8.5 Hz, 1H), 8.03 (d, J=3.3 Hz, 1H), 7.96 (s, 1H), 7.80-7.78 (m, 2H), 7.60 (d, 7.3 Hz, 1H), 7.58 (d, J=7.5 Hz, 1H), 7.25 (td, J=7.5, 1.0 Hz, 1H), 6.88 (d, J=7.8 Hz, 1H), 6.85 (td, J=7.5, 1.0 Hz, 1H); MS ESI 345.1 [M+H]+, calcd for [C19H12N4OS+H]+ 345.07.

Provenance & Evidence