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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantBenzyl isocyanideHCID 82558—
Reactant(+)-Methoxyphenylacetic acidHCID 643325—
Reactant(2-Amino-4,5-difluoro-phenyl)-carbamic acidHCID 86640864—
Solvent1,4-DioxaneHCID 31275—
ProductN-Benzyl-2-cyclohexyl-2-[5,6-difluoro-2-((S)-methoxy-phenyl-methyl)-benzoimidazol-1-yl]-acetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143422B2
Source datasetuspto-grants-2012_03
ORD IDord-1ad4cdf1cb3a4225a0a011929abc171e
Source noteuspto-grants-2012_03