HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922130Generated: November 1, 2026
Triethylamine → Methyl 1-{[(4'-chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetyl]amino}-4-methoxy-4-(trifluoromethyl)cyclohexanecarboxylate
https://huagongshe.com/reaction/922130
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 1-amino-4-methoxy-4-(trifluoromethyl)cyclohexanecarboxylate | HCID 71246475 | — |
| Reactant | (4'-Chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetyl chloride | HCID 86676714 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 1-{[(4'-chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetyl]amino}-4-methoxy-4-(trifluoromethyl)cyclohexanecarboxylate | HCID 90413994 | — |
Reaction Steps
20.50 g (80.32 mmol) of methyl 1-amino-4-methoxy-4-(trifluoromethyl)cyclohexanecarboxylate (Example 22A) and 8.13 g (80.32 mmol) of triethylamine were dissolved in 280 ml of dichloromethane. 21.70 g (73.02 mmol) of (4′-chloro-3′-fluoro-4-methylbiphenyl-3-yl)acetyl chloride (Example 4AA), dissolved in 280 ml of dichloromethane, were added dropwise to this solution, and the reaction mixture was stirred at room temperature overnight. For work-up, the mixture was diluted with dichloromethane and the organic phase was washed with aqueous saturated sodium bicarbonate solution and with aqueous 1% strength citric acid. After drying over sodium sulphate, the organic phase was concentrated and the product was dried. This gave 37.05 g (98% of theory) of the title compound as a beige powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278925B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-59d4e33656114151a0f7098d96a35e04 |
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| Source note | uspto-grants-2016_03 |
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