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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888006Generated: November 1, 2026

4-(Morpholin-4-yl)benzoic acid → HCID 9835852, compound

https://huagongshe.com/reaction/888006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Morpholin-4-yl)benzoic acidHCID 345278—
ReactantN-(tert-Butoxycarbonyl)-1,2-phenylenediamineHCID 676311—
SolventDimethylformamideHCID 6228—
ProductHCID 9835852HCID 983585212%

Reaction Steps

A solution of 1-(N-t-butoxycarbonylamino)-2-aminobenzene (Method 17; 104 mg, 0.5 mmol) in DMF (1.6 ml) was added to 4-morpholinobenzoic acid (149 mg, 0.5 mmol) followed by 4-(4,6-dimethoxy-1,3,5-triazinyl-2-yl)-4-methylmorpholinium chloride (Method 18, 138 mg, 0.5 mmol) and the reaction mixture stirred at ambient temperature for 48 hours. The solvent was removed in vacuo and the resultant residue partitioned between ethyl acetate and water. The organic phase was separated, then washed with water, brine and dried over sodium sulfate then filtered. The organic extracts were concentrated by half and a 4M solution of hydrogen chloride in 1,4-dioxane (1 ml) added. The reaction mixture was stirred at ambient temperature for a further 64 hours and the resultant precipitate was collected by filtration. This solid was purified by preparative mass triggered HPLC, eluting with an increasing gradient of acetonitrile in water (which contains 5% (v/v) of a 1% (v/v) solution of formic acid in methanol) to afford the title compound (17 mg, 12%); NMR Spectrum: (DMSO-d6) 3.25 (m, 4H), 3.76 (m, 4H), 4.83 (s, 2H), 6.60 (m, 1H), 6.79 (dd, 1H), 6.96 (m, 1H), 7.01 (d, 2H), 7.16 (dd, 1H), 7.90 (d, 2H), 9.31 (brs, 1H); Mass Spectrum: M+H+ 298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247562B2
Source datasetuspto-grants-2012_08
ORD IDord-bcff7ec5dd464c898c15d5417f2a7330
Source noteuspto-grants-2012_08