HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Cyclobutyl-6-ethynylpyridazin-3-amine → HCID 72950081, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Cyclobutyl-6-ethynylpyridazin-3-amine | HCID 86709554 | — |
| Reactant | 4-chloro-3-iodo-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide | HCID 86709563 | — |
| Product | HCID 72950081 | HCID 72950081 | — |
Reaction Steps
The title compound was synthesized from N-cyclobutyl-6-ethynylpyridazin-3-amine and 4-chloro-3-iodo-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide in a manner similar to that described for in Example 1. The product was obtained as a pale yellow solid. Mp: 153-155° C.; 1H NMR (300 MHz, CDCl3) δ: 10.34 (1H, s), 8.36 (1H, s), 8.24-8.27 (1H, d, J=8.1 Hz), 8.03 (1H, s), 7.82-7.85 (1H, d, J=8.1 Hz), 7.48 (1H, s), 7.41-7.44 (1H, d, J=8.7 Hz), 7.34-7.37 (2H, t, J=9.3 and 8.7 Hz), 6.80 (1H, s), 6.61-6.64 (1H, d, J=9.6 Hz), 5.57-5.59 (1H, d, J=6.0 Hz), 4.22-4.29 (1H, m), 2.45-2.48 (2H, m), 2.28 (3H, s), 1.76-2.01 (4H, m). HRMS (ESI-TOF+): m/z [M+2H]+2 calcd for C28H24ClF3N6O: 276.0821. found: 276.0817.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859553B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-808d3e07603344b8ad9dd447a3857f40 |
| Source note | uspto-grants-2014_10 |