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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108683Generated: October 30, 2026

2-Aminobenzophenone → HCID 57632408, compound

https://huagongshe.com/reaction/2108683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzophenoneHCID 76080—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57632408HCID 5763240890.2%

Reaction Steps

To a cooled (−78° C.) solution of 2,4-dichloro-5-nitropyrimidine (0.53 g, 2.75 mmol) in THF (3 mL) was added a solution of (2-aminophenyl)(phenyl)methanone (0.30 g, 1.55 mmol) and N,N-diisopropylethylamine (0.5 mL, 3.0 mmol) in THF (2.0 mL). The reaction was stirred for 2.0 hours. The reaction was then poured onto ice and allowed to warm to room temperature then was filtered, washing the solid with water. The isolated solid was dried under vacuum to give {2-[(2-chloro-5-nitropyrimidin-4-yl)amino]phenyl}(phenyl)methanone (496 mg, 90%) as a yellow solid. 1H NMR (DMSO-d6/D2O): δ 9.06 (s, 1H), 7.96 (d, 1H), 7.76-7.44 (m, 8 H). MS m/z 354 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514446B2
Source datasetuspto-grants-2009_04
ORD IDord-9614e4195e67429cb4ba51511c27d41a
Source noteuspto-grants-2009_04