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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712182Generated: October 25, 2026

Hydrochloric Acid → HCID 42605479, compound

https://huagongshe.com/reaction/1712182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant2-Chlorophenoxyacetic acidHCID 11969—
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantCyclohexyl isocyanideHCID 79129—
Reactanttert-Butyl (2-amino-4,5-difluorophenyl)carbamateHCID 66619231—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 42605479HCID 4260547934%

Reaction Steps

To a solution of (2-amino-4,5-difluoro-phenyl)-carbamic acid tert-butyl ester (24.42 mg, 0.10 mmol, 1.0 equiv; Intermediate C) 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 pi, 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 I water provided 17.5 mg (34%) of the title compound. MS (ISP): 516.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790904B2
Source datasetuspto-grants-2010_09
ORD IDord-cef23f7fe806428fb7397ea46f8a11af
Source noteuspto-grants-2010_09