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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396193Generated: November 2, 2026

4-((4-Methylpiperazin-1-yl)methyl)aniline → HCID 66576945, compound

https://huagongshe.com/reaction/1396193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
ReactantHCID 86673362HCID 86673362—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 66576945HCID 6657694593%

Reaction Steps

The title compound was prepared according to synthesis procedure B described above from 5-(2-chloro-5-methylpyrimidin-4-yl)-2-methylbenzonitrile and 4-((4-methylpiperazin-1-yl)methyl)aniline in 93% yield (yellow solid). After flash chromatography (CH2Cl2/CH3OH 99:1 gradually increasing to 95:5). 1H NMR (400 MHz, CDCl3): δ 8.31 (s, 1H), 7.88 (d, 1H, J=1.7 Hz), 7.76 (dd, 1H, J=8.0, 1.9 Hz), 7.55 (d, 2H, J=8.6 Hz), 7.43 (d, 1H, J=7.9 Hz), 7.25 (d, 2H, J: not calculated due to overlapping peaks), 3.45 (s, 2H), 2.62 (s, 3H), 2.45 (bs, 8H), 2.26 (s, 3H), 2.25 (s, 3H); MS (ESI): 413.5 [M+H]+, 207.4 [M+2H]2+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901120B2
Source datasetuspto-grants-2014_12
ORD IDord-0689f86e9a1f4937b085aaaaa04a671d
Source noteuspto-grants-2014_12