HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide → 4-Chloro-3-(2-(6-(cyclopropylamino)pyridazin-3-yl)ethynyl)-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide | HCID 71562635 | — |
| Reactant | N-cyclopropyl-6-ethynylpyridazin-3-amine | HCID 86709556 | — |
| Product | 4-Chloro-3-(2-(6-(cyclopropylamino)pyridazin-3-yl)ethynyl)-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide | HCID 72949911 | — |
Reaction Steps
The title compound was synthesized from N-cyclopropyl-6-ethynylpyridazin-3-amine and 4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl) benzamide in a manner similar to that described for in Example 1. The intermediate compound 4-chloro-3-iodo-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide was made as for Example 12 (Step 1 to 4) with the spectra below: 1H NMR (300 MHz, DMSO-d6) δ: 10.66 (1 H, s), 8.53 (1 H, s), 8.19 (1 H, s), 8.02-8.05 (1 H, d, J=6.0 Hz), 7.98-8.01 (1 H, d, J=6.0 Hz), 7.77 (1 H, s), 7.70-7.73 (1 H, d, J=6.0 Hz), 3.62 (2 H, s), 3.33 (2 H, m), 2.82 (2 H, m), 2.54 (4 H, m), 2.50 (3 H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174996B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-76ed2edfc8fa4d91b7e3dc02fb2aef72 |
| Source note | uspto-grants-2015_11 |