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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711379Generated: November 4, 2026

3-Acetylbenzoic acid → HCID 67200176, compound

https://huagongshe.com/reaction/1711379

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Acetylbenzoic acidHCID 220324—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 59457979HCID 59457979—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 67200176HCID 67200176—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of N4-(4-Aminophenyl)-N6,N6-dimethyl-4,6-quinolinediamine (181 mg, 0.58 mmol), 3-acetylbenzoic acid (M1) (97 mg, 0.58 mmol) and EDCl (220 mg, 0.1.16 mmol) in DMF (5 mL) was stirred at 20° C. for 5 min. Then DMAP (140 mg, 1.16 mmol) was added and the reaction mixture was stirred at 20° C. for 24 h. The solvent was removed under reduced pressure and residue was stirred in aqueous NaHCO3 for 1 h. The resulting precipitate was filtered and purified by chromatography in SiO2 eluting with a gradient (0-7.5%) of MeOH/DCM to give M2 (113 mg, 42%); mp (DCM/MeOH)>280° C.; 1H NMR [(CD3)2SO] δ 14.02 (br, 1H, N+H), 10.66 (s, 1H, NH), 10.31 (s, 1H, NH), 8.53 (t, J=1.6 Hz, 1H, ArH), 8.28 (d, J=6.7 Hz, 1H, ArH), 8.24 (td, J=8.1, 1.5 Hz, 1H, ArH), 8.19 (td, J=7.8, 2.8 Hz, 1H, ArH), 8.00 (d, J=6.8 Hz, 2H, ArH), 7.87 (d, J=9.4 Hz, 1H, ArH), 7.78 (t, J=7.8 Hz, 1H, ArH), 7.64 (dd, J=9.4, 2.6 Hz, 1H, ArH), 7.51 (d, J=2.5 Hz, 1H, ArH), 7.47 (d, J=8.8 Hz, 2H, ArH), 6.69 (d, J=6.7 Hz, 1H, ArH), 3.09 [s, 6H, (NCH3)2], 2.68 (s, 3H, COCH3); APCl+ve 425.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790746B2
Source datasetuspto-grants-2010_09
ORD IDord-47afaf43a8954f4db722d530ddd17b46
Source noteuspto-grants-2010_09