Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712183Generated: October 26, 2026

Hydrochloric Acid → HCID 42606856, compound

https://huagongshe.com/reaction/1712183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantCyclohexanecarboxaldehydeHCID 16275—
Reactant(4-Chlorophenoxy)acetic acidHCID 26229—
ReactantCyclohexyl isocyanideHCID 79129—
Reactanttert-Butyl (2-amino-4-chloro-5-fluorophenyl)carbamateHCID 67375046—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 42606856HCID 4260685637%

Reaction Steps

To a solution of (2-amino-4-chloro-5-fluoro-phenyl)-carbamic acid tert-butyl ester (26.07 mg, 0.10 mmol, 1.0 equiv; Intermediate D) in MeOH (1.0 mL) was added cyclohexanecarbaldehyde (16.83 mg, 18.05 1, 0.15 mmol, 1.5 equiv; [2043-61-0]) and the mixture stirred at rt. After 30 min, (4-chloro-phenoxy)-acetic acid (18.66 mg, 0.10 mmol, 1.0 equiv; [CAS RN 122-88-3]) and cyclohexyl isocyanide (10.92 mg, 12.27 1, 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 19.6 mg (37%) of the title compound. MS (ISP): 532.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790904B2
Source datasetuspto-grants-2010_09
ORD IDord-5b5bdbce63a344b7806fa7357f5b568f
Source noteuspto-grants-2010_09