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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261959Generated: November 3, 2026

1-(4-Nitrophenyl)piperazine → HCID 66712003, compound

https://huagongshe.com/reaction/1261959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
Reactant1-(3-Nitrophenyl)piperazineHCID 2760216—
ReactantHCID 66710773HCID 66710773—
Reactant2-Methanesulfinyl-7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazineHCID 66710791—
ProductHCID 66712003HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-edd018a24e0348d3aed64c5897f2fea9
Source noteuspto-grants-2013_06