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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190868Generated: October 31, 2026

Hydrochloric Acid → 3-[(Tert-butylamino)methyl]-4-(4-methylpiperazin-1-yl)aniline

https://huagongshe.com/reaction/1190868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
ReactantStannous ChlorideHCID 24479—
ReactantTert-butyl({[2-(4-methylpiperazin-1-yl)-5-nitrophenyl]methyl})amineHCID 67247988—
SolventTetrahydrofuranHCID 8028—
Product3-[(Tert-butylamino)methyl]-4-(4-methylpiperazin-1-yl)anilineHCID 6724782449%

Reaction Steps

A mixture of SnCl2 (0.364 g, 4 eq), 1.44 mL of HCl 1M and 5 mL of THF was added to a solution of tert-butyl({[2-(4-methylpiperazin-1-yl)-5-nitrophenyl]methyl})amine (0.147 g, 0.48 mmol) in 20 mL of THF. The reaction mixture was refluxed for 3 h and allowed to cool to room temperature. A saturated aqueous solution of Na2CO3 was added. The aqueous layer was extracted with DCM. The combined organic layers were dried over Na2SO4, filtered and evaporated. The residue was purified by flash chromatography (DCM/MeOH/NH4OH//85/15/1) to yield expected compound as a brown oil (65 mg, 49% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680095B2
Source datasetuspto-grants-2014_03
ORD IDord-fa47b8900ed54bf59f7c1b252ef1d3ce
Source noteuspto-grants-2014_03