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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633368Generated: October 26, 2026

Water → {2-[(3-Aminopyridin-2-yl)amino]phenyl}(3-fluorophenyl)methanone

https://huagongshe.com/reaction/1633368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(3-Fluorophenyl){2-[(3-nitropyridin-2-yl)amino]phenyl}methanoneHCID 13388388—
Catalysttitanium(III) trichlorideHCID 10313229—
SolventAcetic acid ethanolHCID 18476134—
SolventAcetic acid--water (1/1)HCID 21899381—
Product{2-[(3-Aminopyridin-2-yl)amino]phenyl}(3-fluorophenyl)methanoneHCID 1338839149.3%

Reaction Steps

Under an atmosphere of nitrogen, 30 g of titanium trichloride was added portionwise (cautiously) with stirring to 200 ml of ice. The resulting solution was added all at once to a stirred solution of 10.0 g (0.0297 mole) of (3-fluorophenyl)[2-[(3-nitro-2-pyridinyl)amino]phenyl]methanone in 150 ml of acetic acid: ethanol (1:1) and 150 ml of acetic acid: water (1:1). After 30 min stirring, the reaction mixture was poured into one liter of water. The mixture was filtered and the resulting filter-cake was suspended in 100 ml of water. The mixture was again filtered and the filter-cake (10.0 g) was partially dissolved in 100 ml of hot methanol. The solution was basified with 25 ml of concentrated ammonium hydroxide, stirred for an additional 15 min and then diluted with 500 ml of water. The mixture was extracted three times with 75 ml portions of methylene chloride. The combined methylene chloride extracts were washed with 50 ml of water, dried over sodium sulfate and concentrated in vacuo. The residue (6.9 g) was twice recrystallized, treating once with charcoal, from ethyl acetate-isopropyl ether to give 4.5 g (49%) of a dark gold solid, m.p. 135°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04480100
Source datasetuspto-grants-1984_10
ORD IDord-3fbed1dbd6b84bf69dbbafd43bbfa42f
Source noteuspto-grants-1984_10