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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637453Generated: November 4, 2026

2-Aminobenzophenone → HCID 135626384, compound

https://huagongshe.com/reaction/637453

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzophenoneHCID 76080—
Reactant2-Chloro-3-pyridylamineHCID 80528—
ProductHCID 135626384HCID 13562638426.9%

Reaction Conditions

Temperature190 °C

Reaction Steps

A mixture of 19.7 g (0.1 mole) of 2-aminobenzophenone and 15.0 g (0.12 mole) of 3-amino-2-chloropyridine was heated under nitrogen atmosphere at 190° C. for 1.75 hr. The mixture was cooled to room temperature and partitioned between 3N aqueous sodium hydroxide and methylene chloride. The combined methylene chloride extracts were washed with water, dried over magnesium sulfate and evaporated under reduced pressure. The residue, 32.7 g, was dissolved in benzene and chromatographed on a column of florisil packed in benzene, eluting with benzene and 1-2% acetone-benzene mixtures. After evaporation, the solid was crystallized from benzene to give 7.3 g product; m.p. 106°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556667
Source datasetuspto-grants-1985_12
ORD IDord-e02838f5bb664e4eb074e852627e1e95
Source noteuspto-grants-1985_12