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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Cyclohexylaniline | HCID 74567 | — |
| Reactant | 5-Bromo-2,4-dichloropyrimidine | HCID 289973 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | (5-Bromo-2-chloro-pyrimidin-4-yl)-cyclohexyl-phenyl-amine | HCID 58299589 | 24% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841312B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-6e09e02edeb2407fa29c35bb3c7b1f63 |
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| Source note | uspto-grants-2014_09 |
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