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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261952Generated: November 2, 2026

1-(4-Nitrophenyl)piperazine → HCID 66711038, compound

https://huagongshe.com/reaction/1261952

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 66711038HCID 66711038—

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-(3-Chloro-phenyl)-2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazine to afford 22.28 mg of (R)-1-(4-{3-[7-(3-Chloro-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-ylamino]-phenyl}-piperazin-1-yl)-propan-2-ol as a lyophilized powder. (M+H)=463.12. 1H NMR (400 MHz, DMSO, d6) δ 9.52 (m, 1H), 9.41 (s, 1H), 8.39 (m, 1H), 8.06 (d, 1H, J=7.68 Hz), 7.50 (m, 3H), 7.25 (m, 2H), 7.18 (m, 1H), 6.97 (d, 1H, J=4.76 Hz), 6.67 (d, 1H, J=8.00 Hz), 4.11 (m, 2H), 3.66 (m, 2H), 3.53 (m, 2H), 3.14 (m, 3H), 3.03 (m, 2H), 1.15 (d, 3H, J=6.16 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-ce39fa9704c440f78fac1a2d2f1d4475
Source noteuspto-grants-2013_06