HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054196Generated: November 1, 2026
4-tert-Butylcyclohexylamine → HCID 178445674, compound
https://huagongshe.com/reaction/2054196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylcyclohexylamine | HCID 79396 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Chloro-4-(4-pyridinylmethyl)phthalazine | HCID 1944609 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178445674 | HCID 178445674 | — |
Reaction Steps
A mixture of 1.0 g (3.91 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine (Example 67.A1 in WO 98/35958) and 1.82 g (11.7 mmol) 4-tert-butylcyclohexylamine (trans-/cis-mixture) is stirred overnight at 120° C. The cooled reaction mixture is then distributed between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The organic phase is washed with water and brine, dried (MgSO4) and evaporated and the residue purified on silica gel by flash chromatography using dichloromethane/methanol (9:1) yielding the title compound as a trans-/cis-mixture: FAB MS (M+H)+=375. Separation of the isomers by reversed phase medium pressure chromatography (CH3CN/H2O/trace of TFA) gives the cis-isomer (m.p. 64-65° C.) followed by the trans-isomer (m.p. 132-134° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07329660B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-8e7f706386ee483aa9c064b1cbb3aa64 |
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| Source note | uspto-grants-2008_02 |
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