HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Nitrophenyl)piperazine → HCID 66712003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Reactant | 1-(3-Nitrophenyl)piperazine | HCID 2760216 | — |
| Reactant | HCID 66710773 | HCID 66710773 | — |
| Reactant | 2-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazine | HCID 66710791 | — |
| Product | HCID 66712003 | HCID 66712003 | — |
Reaction Steps
The compound was prepared in an analogous fashion to Example 85 replacing 1-(3-Nitro-phenyl)-piperazine with 1-(4-Nitro-phenyl)-piperazine and 2-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazine with 7-(3-Chloro-phenyl)-2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazine to afford 22.28 mg of 1-(4-{4-[7-(3-Chloro-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-phenyl}-piperazin-1-yl)-2-methyl-propan-2-ol as a lyophilized powder. (M+H)=477.8. 1H NMR (400 MHz, DMSO, d6) δ 9.39 (s, 1H), 8.99 (s, 1H), 8.49 (s, 1H), 8.03 (d, 1H, J=7.93 Hz), 7.67 (d, 2H, J=8.92 Hz), 7.54 (t, 1H, J=7.97 Hz), 7.44 (m, 1H), 7.26 (d, 1H, J=4.76 Hz), 7.01 (d, 2H, J=8.96 Hz), 6.95 (d, 1H, J=4.76 Hz), 3.63 (m, 4H), 3.25 (m, 6H), 1.31 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08471005B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-edd018a24e0348d3aed64c5897f2fea9 |
| Source note | uspto-grants-2013_06 |