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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396186Generated: November 2, 2026

4-((4-Methylpiperazin-1-yl)methyl)aniline → HCID 66576708, compound

https://huagongshe.com/reaction/1396186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
ReactantHCID 86673359HCID 86673359—
ProductHCID 66576708HCID 6657670884%

Reaction Steps

The title compound was prepared according to synthesis procedure B described above from 2-chloro-4-(3-chloro-4-fluorophenyl)-5-methylpyrimidine and 4-((4-methylpiperazin-1-yl)methyl)aniline in 84% yield (yellow solid) after purification by flash chromatography (CH2Cl2/CH3OH 99:1 gradually increasing to 95:5). 1H NMR (400 MHz, CDCl3): δ 8.30 (s, 1H), 7.70 (m, 1H), 7.56 (d, 2H, J=8.6 Hz), 7.51 (m, 1H), 7.25 (d, 2H, J: not calculated due to overlapping peaks), 7.05 (s, 1H), 3.46 (s, 2H), 2.46 (bs, 8H), 2.28 (s, 3H), 2.25 (s, 3H); MS (ESI): 426.3 [M+H]+, 213.7 [M+2H]2+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901120B2
Source datasetuspto-grants-2014_12
ORD IDord-a06eaa661ec14293a49d1140e7fb1380
Source noteuspto-grants-2014_12