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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262238Generated: November 2, 2026

3-(4-Aminophenyl)-1,4-dimethylpiperazin-2-one → HCID 66711745, compound

https://huagongshe.com/reaction/1262238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Aminophenyl)-1,4-dimethylpiperazin-2-oneHCID 57625120—
ReactantHCID 178449976HCID 178449976—
ProductHCID 66711745HCID 66711745—

Reaction Steps

N-tert-Butyl-3-{2-[4-(1,4-dimethyl-3-oxo-piperazin-2-yl)-phenylamino]-pyrrolo[2,1-f][1,2,4]triazin-7-yl}-benzenesulfonamide was prepared from N-tert-butyl-3-(2-hydroxy-pyrrolo[2,1-f][1,2,4]triazin-7-yl)-benzenesulfonamide and 3-(4-amino-phenyl)-1,4-dimethyl-piperazin-2-one in an analogous manner to Example 1052a. Product isolated as an orange foam (90 mg, 56%). LCMS (m/e) 548 (M+H); 1H-NMR (CDCl3, 400 MHz) δ 8.97 (s, 1H), 8.74 (s, 1H), 8.21 (d, 1H, J=7.9 Hz), 7.89 (d, 1H, J=7.8 Hz), 7.64-7.54 (m, 3H), 7.42 (d, 2H, J=8.3 Hz), 7.10 (d, 1H, J=4.8 Hz), 6.91-6.83 (m, 2H), 4.86 (s, 1H), 3.83-3.70 (m, 2H), 3.27-3.17 (m, 1H), 3.04 (s, 3H), 3.06-2.98 (m, 1H), 2.75-2.65 (m, 1H), 2.21 (s, 3H), 1.14 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-df95e86659974167a0a0b42b0e050c87
Source noteuspto-grants-2013_06