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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396194Generated: November 3, 2026

4-((4-Methylpiperazin-1-yl)methyl)aniline → HCID 66576867, compound

https://huagongshe.com/reaction/1396194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
ReactantHCID 86673363HCID 86673363—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 66576867HCID 6657686782%

Reaction Steps

The title compound was prepared according to synthesis procedure B described above from N-(3-(2-chloro-5-methylpyrimidin-4-yl)phenyl)acetamide and 4-((4-methylpiperazin-1-yl)methyl)aniline in 82% yield (yellow solid) after flash chromatography (CH2Cl2/CH3OH 99:1 gradually increasing to 95:5). 1H NMR (400 MHz, CDCl3): δ 8.29 (s, 1H), 7.79 (s, 1H), 7.57 (d, 3H, J=8.2 Hz), 7.42 (t, 1H, J=7.9 Hz), 7.35 (d, 1H, J=7.5 Hz), 7.22 (m, 2H), 3.44 (s, 2H), 2.42 (bs, 8H), 2.26 (s, 3H), 2.19 (s, 3H); (ESI): 431.3 [M+H]+, 216.3 [M+2H]2±.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901120B2
Source datasetuspto-grants-2014_12
ORD IDord-ce728f1826da4fe38d7b88cd651f9624
Source noteuspto-grants-2014_12