HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099465Generated: November 2, 2026
Hydrochloric Acid → N-Benzyl-2-cyclohexyl-2-[5,6-difluoro-2-((S)-methoxy-phenyl-methyl)-benzoimidazol-1-yl]-acetamide
https://huagongshe.com/reaction/1099465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Reactant | Benzyl isocyanide | HCID 82558 | — |
| Reactant | (+)-Methoxyphenylacetic acid | HCID 643325 | — |
| Reactant | (2-Amino-4,5-difluoro-phenyl)-carbamic acid | HCID 86640864 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-Benzyl-2-cyclohexyl-2-[5,6-difluoro-2-((S)-methoxy-phenyl-methyl)-benzoimidazol-1-yl]-acetamide | HCID 66810470 | — |
Reaction Steps
To a mixture of (2-amino-4,5-difluoro-phenyl)-carbamic acid tent-butyl ester (1.00 g, 4 mmol, 1.0 equiv) and (S)-alpha-methoxyphenylacetic acid (0.68 g, 1.0 equiv., [CAS RN 26164-26-1]) in methanol (25 mL) were added cyclohexanecarbaldehyde (0.459 g, 4 mmol, 1.0 equiv; [2043-61-0]) and benzyl isonitrile (0.48 g, 1.0 equiv., 4 mmol, CAS RN 10340-91-7). The mixture was stirred overnight at room temperature. A solution of 4 M HCl in dioxane (3 mL) was added, and the reaction mixture stirred at room temperature overnight. The mixture was partitioned between water (100 ml) and ethyl acetate (100 ml). The phases were separated and the aqueous phase extracted with ethyl acetate (2×50 ml), the combined organic phases washed with brine, dried over sodium sulfate and evaporated under reduced pressure to afford the title compound as an orange gum (2.16 g, quant., mixture of diastereomers) that was used without further purification. MS (ISP): 504.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143422B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-1ad4cdf1cb3a4225a0a011929abc171e |
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| Source note | uspto-grants-2012_03 |
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