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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463032Generated: October 30, 2026

(4-Chlorophenyl){2-[(3-nitropyridin-2-yl)amino]phenyl}methanone → {2-[(3-Aminopyridin-2-yl)amino]phenyl}(4-chlorophenyl)methanone

https://huagongshe.com/reaction/463032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl){2-[(3-nitropyridin-2-yl)amino]phenyl}methanoneHCID 13388387—
ReactantEthylacetate methanolHCID 21584119—
ReactantAcetic acid--water (1/1)HCID 21899381—
Catalysttitanium(III) trichlorideHCID 10313229—
SolventWaterHCID 962—
Product{2-[(3-Aminopyridin-2-yl)amino]phenyl}(4-chlorophenyl)methanoneHCID 1338839059.4%

Reaction Steps

Under an atmosphere of nitrogen, 29 g (0.187 mole) of titanium trichloride was added portionwise (cautiously; in hood) to 200 g of ice and the resulting solution was diluted to 250 ml volume with water. This was added, all at once, at 30° C. to a stirred solution of 11.0 g (0.0312 mole) of (4-chlorophenyl)[2-[(3-nitro-2-pyridinyl)amino]phenyl]methanone, 300 ml of ethyl acetate:methanol (1:1), 100 ml of acetic acid:water (1:1) and 20 ml more solution of titanium trichloride. The reaction mixture was stirred for 20 min then diluted with one liter of water and filtered. The filter cake was washed with water and then partitioned between 200 ml of methylene chloride and 75 ml of 10% aqueous sodium hydroxide solution. The methylene chloride layer was washed with 75 ml of water, dried over sodium sulfate and concentrated in vacuo. The residue (7 g) was recrystallized from ethyl acetate-isopropyl ether to give 6.0 g of gold solid, m.p. 145°-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518603
Source datasetuspto-grants-1985_05
ORD IDord-f5f4114c6eff4370b6bd31bcf1140309
Source noteuspto-grants-1985_05