HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752066Generated: October 29, 2026
1,2-Diaminocyclohexane, trans- → HCID 57762549, compound
https://huagongshe.com/reaction/1752066
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| Reactant | HCID 22346771 | HCID 22346771 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57762549 | HCID 57762549 | — |
Reaction Steps
Under an argon atmosphere, a suspension of N-(4-bromophenyl)pyrimidin-2-amine (250 mg), copper iodide (1.9 mg), trans-1,2-cyclohexanediamine (0.015 ml) and sodium-tert-butoxide (144 mg) in dioxane (1 ml) was stirred at 110° C. for 22 hours in a pressure-resistant test tube. The reaction solution was filtered and the filtrate was concentrated. The residue was purified by thin layer chromatography (silica gel, mobile phase: chloroform/ethyl acetate=5/1) to obtain N-(4-bromophenyl)-N-phenylpyrimidin-2-amine (56 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09162988B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-3624cf41d8f643e3a3fc67baadb83351 |
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| Source note | uspto-grants-2015_10 |
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