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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660133Generated: October 31, 2026

Hydrochloric Acid → HCID 178522244, compound

https://huagongshe.com/reaction/660133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantSodium hydrideHCID 24758—
ReactantO,O-Dipyridin-2-yl carbonothioateHCID 719784—
Reactant3-Amino-5-fluorobenzotrifluorideHCID 2735913—
ReactantHCID 178472469HCID 178472469—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178522244HCID 17852224444.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

Sodium hydride (60% dispersion in mineral oil, 192 mg, 4.80 mmol) was added to a stirred solution of 3-amino-5-fluorobenzotrifluoride (430 mg, 2.40 mmol) in DMF (10 mL) at ambient temperature. After 5 mins di-2-pyridyl thionocarbonate (557 mg, 2.40 mmol) was added in one portion and stirring was continued for 10 mins. Ethyl cis-4-(4-{[hydrazino(oxo)acetyl]amino}phenoxy)cyclohexanecarboxylate (Intermediate 1, 698 mg, 2.00 mmol) was added in one portion to the reaction mixture and stirred at 65° C. for 30 mins. EDCI (460 mg, 2.40 mmol) was then added in one portion and the reaction mixture was heated to 85° C. for 3 h. The mixture was cooled to ambient temperature and water (15 mL) was added and the resulting suspension was filtered to leave a cream solid. The solid was taken up in a mixture of MeOH (8 mL) and THF (4 mL) and a 2N aqueous solution of NaOH (4 mL) was added in one portion and the reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was acidified by the addition of 2M HCl and the resulting precipitate was filtered, washed with water (10 mL) and dried under high vacuum to leave a solid. The solid was recrystallised from refluxing glacial acetic acid to provide the title compound as a white solid (448 mg, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084478B2
Source datasetuspto-grants-2011_12
ORD IDord-dc311c494aa1429083189bf23d9a43fe
Source noteuspto-grants-2011_12