HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261951Generated: November 4, 2026
1-(4-Nitrophenyl)piperazine → HCID 66711040, compound
https://huagongshe.com/reaction/1261951
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Reactant | 1-(3-Nitrophenyl)piperazine | HCID 2760216 | — |
| Reactant | 2-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazine | HCID 66710791 | — |
| Reactant | HCID 66710941 | HCID 66710941 | — |
| Product | HCID 66711040 | HCID 66711040 | — |
Reaction Steps
The compound was prepared in an analogous fashion to Example 73 replacing 1-(4-Nitro-phenyl)-piperazine with 1-(3-Nitro-phenyl)-piperazine and 2-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazine with 7-(5-Chloro-2-methoxy-phenyl)-2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazine to afford 19.24 mg of (R)-1-(4-{3-[7-(5-Chloro-2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-phenyl}-piperazin-1-yl)-propan-2-ol as a lyophilized powder. (M+H)=493.09. 1H NMR (400 MHz, DMSO, d6) δ 9.34 (s, 1H), 8.98 (s, 1H), 7.94 (m, 1H), 7.50 (dd, 1H, J=2.64, 6.24 Hz), 7.39 (d, 1H, J=8.12 Hz), 7.24 (d, 1H, J=8.96 Hz), 7.14 (m, 2H), 7.01 (d, 1H, J=4.68 Hz), 6.93 (d, 1H, J=4.68 Hz), 6.59 (dd, 1H, J=1.80, 6.48 Hz), 4.12 (m, 2H), 3.80 (s, 3H), 3.53 (m, 4H), 3.15 (m, 3H), 3.02 (m, 2H), 1.15 (d, 2H, J=6.16 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08471005B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-2488d276e8124bf5b5b384df783008cd |
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| Source note | uspto-grants-2013_06 |
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