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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712181Generated: October 25, 2026

Hydrochloric Acid → 2-[2-(2-Chloro-phenoxymethyl)-5-fluoro-benzoimidazol-1-yl]-2,N-dicyclohexyl-acetamide

https://huagongshe.com/reaction/1712181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant2-Chlorophenoxyacetic acidHCID 11969—
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantCyclohexyl isocyanideHCID 79129—
ReactantN2-(tert-Butoxycarbonyl)-4-fluoro-1,2-phenylenediamineHCID 53420357—
Solvent1,4-DioxaneHCID 31275—
Product2-[2-(2-Chloro-phenoxymethyl)-5-fluoro-benzoimidazol-1-yl]-2,N-dicyclohexyl-acetamideHCID 4260627113%

Reaction Steps

To a solution of (2-amino-5-fluoro-phenyl)-carbamic acid tert-butyl ester (22.63 mg, 0.10 mmol, 1.0 equiv, Intermediate B) in MeOH (1.0 mL) was added cyclohexanecarbaldehyde (16.83 mg, 18.05 μl 0.15 mmol, 1.5 equiv; [2043-61-0]) and the mixture stirred at rt. After 30 min, (2-chloro-phenoxy)-acetic acid (18.66 mg, 0.10 mmol, 1.0 equiv; [CAS RN 614-61-9]) and cyclohexyl isocyanide (10.92 mg, 12.27 μl, 0.10 mmol, 1.0 equiv; [931-53-3]) were added and stirring continued at rt for 2 h. A solution of 4 M HCl in dioxane (0.2 mL) was added and the reaction mixture stirred at rt overnight. Removal of the solvent mixture under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 6.3 mg (13%) of the title compound. MS (ISP): 498.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790904B2
Source datasetuspto-grants-2010_09
ORD IDord-73d82f2a1a35435ab9625fc36c23c8ae
Source noteuspto-grants-2010_09