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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402835Generated: October 25, 2026

Potassium cyanate → N-{2-(Carbamoylamino)-1-[3-(trifluoromethyl)phenyl]ethyl}-2-{3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}acetamide

https://huagongshe.com/reaction/2402835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium cyanateHCID 11378442—
ReactantN-{2-Amino-1-[3-(trifluoromethyl)phenyl]ethyl}-2-{3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}acetamide hydrochlorideHCID 46929233—
SolventMethanol--water (1/1)HCID 22242641—
ProductN-{2-(Carbamoylamino)-1-[3-(trifluoromethyl)phenyl]ethyl}-2-{3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}acetamideHCID 59536760—

Reaction Conditions

Temperature40 °C

Reaction Steps

Of the compound from Example 11, 266 mg (0.45 mmol) were introduced in 6 ml of methanol/water 1:1 and admixed with potassium cyanate (110 mg, 1.36 mmol) at RT. The mixture was heated at 40° C. for 90 min. Following complete reaction, the mixture was cooled to RT and purified completely by preparative HPLC (Method 10). Drying in an HV gave 232 mg (84% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796324B2
Source datasetuspto-grants-2014_08
ORD IDord-aa3f242f2f644988857c1a2cfbe2db55
Source noteuspto-grants-2014_08