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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888013Generated: November 2, 2026

N-(tert-Butoxycarbonyl)-1,2-phenylenediamine → HCID 68406951, compound

https://huagongshe.com/reaction/888013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-Butoxycarbonyl)-1,2-phenylenediamineHCID 676311—
Reactant4-[4-(tert-Butoxycarbonyl)piperazin-1-yl]benzoic acidHCID 2795508—
SolventDimethylformamideHCID 6228—
ProductHCID 68406951HCID 6840695192%

Reaction Steps

To a solution of 4-(4-t-butoxycarbonylpiperazin-1-yl)benzoic acid (1.0 g, 3.3 mmol) and 1-(t-butoxycarbonylamino)-2-aminobenzene (Method 17, 0.68 g, 3.3 mmol) in DMF (10 ml) was added 4-(4,6-dimethoxy-1,3,5-triazinyl-2-yl)-4-methylmorpholinium chloride (1.1 g, 4.0 mmol) (Method 18). The mixture was stirred at ambient temperature for 20 hours. The mixture was concentrated in vacuo and the residue partitioned between water and ethyl acetate. The organic phase was separated and the aqueous reextracted with ethyl acetate. The combined organic extracts were dried over magnesium sulfate and evaporated. The residue was purified by flash chromatography (eluting with 4:1-1:1 isohexane/ethyl acetate). The product was dissolved in 1,4-dioxane (2.5 ml) and treated with a 4M solution of hydrogen chloride in 1,4-dioxane (2.5 ml). The mixture was stirred at ambient temperature for 4 hours. The resulting solid was collected by filtration, trated with a 2M aqueous solution of sodium hydroxide and extracted with ethyl acetate. The organic extract was dried over magnesium sulfate to afford the title compound as a colourless solid (176 mg, 92%); NMR Spectrum: (DMSO-d6) 2.89 (t, 4H), 3.25 (t, 4H), 4.90 (s, 2H), 6.66 (t, 1H), 6.84 (d, 1H), 7.01 (m, 3H), 7.21 (d, 1H), 7.92 (d, 2H), 9.48 (s, 1H); Mass Spectrum: M+H+ 297.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247562B2
Source datasetuspto-grants-2012_08
ORD IDord-570fdc2004584f8296ca1eac5e52d32e
Source noteuspto-grants-2012_08