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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79113Generated: October 23, 2026

N-Cyclohexylaniline → (5-Bromo-2-chloro-pyrimidin-4-yl)-cyclohexyl-phenyl-amine

https://huagongshe.com/en/reaction/79113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-CyclohexylanilineHCID 74567—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(5-Bromo-2-chloro-pyrimidin-4-yl)-cyclohexyl-phenyl-amineHCID 5829958924%

Reaction Conditions

Temperature120 °C

Reaction Steps

5-Bromo-2,4-dichloro-pyrimidine (2.17 ml, 17.14 mmol) and cyclohexyl-phenyl-amine (2.0 g, 11.43 mmol) were dissolved in N-methylpyrrolidone (NMP) (25 ml), and this reaction was heated to 120° C. for 24 hours. The reaction was cooled to room temperature and diluted with ethyl acetate, washed with water and brine. The organic phase was dried using sodium sulfate and concentrated. Purification by flash chromatography (ethyl acetate/hexane) gave compound 37 as a yellow solid (855 mg, 24%). 1H NMR (500 MHz, DMSO-d6) δ ppm 8.27 (1 H, s), 7.41 (3 H, m), 7.21 (2 H, m), 4.62 (1 H, m), 1.93 (2 H, d, J=10 Hz), 1.75 (2 H, d, J=10 Hz), 1.58 (1 H, d, J=10 Hz), 1.34 (2 H, m), 1.15 (2 H, m), 0.91 (1 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841312B2
Source datasetuspto-grants-2014_09
ORD IDord-6e09e02edeb2407fa29c35bb3c7b1f63
Source noteuspto-grants-2014_09