HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70339Generated: October 29, 2026
Triethylamine → 3'-({2-[(4,4-Dimethylcyclohexyl)amino]ethyl}oxy)-4-biphenylcarboxamide hydrochloride
https://huagongshe.com/reaction/70339
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,4-Dimethylcyclohexanamine hydrochloride | HCID 24191928 | — |
| Reactant | 3'-[(2-Bromoethyl)oxy]-4-biphenylcarboxamide | HCID 58276262 | — |
| Reactant | 3'-[(2-Chloroethyl)oxy]-4-biphenylcarboxamide | HCID 58276352 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3'-({2-[(4,4-Dimethylcyclohexyl)amino]ethyl}oxy)-4-biphenylcarboxamide hydrochloride | HCID 67160430 | — |
Reaction Steps
A mixture of 3′-[(2-chloroethyl)oxy]-4-biphenylcarboxamide and 3′-[(2-bromoethyl)oxy]-4-biphenylcarboxamide (Example II-1) (0.15 g), 4,4-dimethylcyclohexylamine hydrochloride (0.13 g, 0.8 mmol) (prepared according to J. Med. Chem. 1971, 14, p. 600-614) and triethylamine (0.14 g, 1.35 mmol) in methanol (2 mL) was placed in a microwave at 160° C. until the reaction was complete as monitored by LC/MS. The reaction mixture was poured into ethyl acetate and washed several times with 5% Na2CO3 (aq). Silica gel was added to the organic phase and the mixture was concentrated in vacuo. The residue was purified by silica gel chromatography. The fractions containing the desired product were combined and concentrated in vacuo. Dissolved the residue in ethanol, added 1.0N HCl in Et2O until acidic, added ethyl ether until turbid and let stand at room temperature. The resulting solid was filtered, washed with ethyl ether and dried to give 3′-({2-[(4,4-dimethylcyclohexyl)amino]ethyl}oxy)-4-biphenylcarboxamide hydrochloride as an off-white solid. (M+H) 367, 1.83 min. (LC/MS method A)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822518B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-31192e4280154abaa3955ea51a10d8f0 |
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| Source note | uspto-grants-2014_09 |
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