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

HRID 2402835

Reaktionsgleichung

Cl.[NH2:2][CH2:3][CH:4]([NH:15][C:16](=[O:38])[CH2:17][N:18]1[C:22](=[O:23])[N:21]([CH2:24][C@H:25]([OH:30])[C:26]([F:29])([F:28])[F:27])[C:20]([C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=2)=[N:19]1)[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1.[O-:39][C:40]#[N:41].[K+]>CO.O>[C:40]([NH:2][CH2:3][CH:4]([NH:15][C:16](=[O:38])[CH2:17][N:18]1[C:22](=[O:23])[N:21]([CH2:24][C@H:25]([OH:30])[C:26]([F:29])([F:27])[F:28])[C:20]([C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=2)=[N:19]1)[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:12])([F:14])[F:13])[CH:6]=1)(=[O:39])[NH2:41]

Komponenten

Reaktionsbedingungen

Temperatur: 40 °C

Versuchsvorschrift

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.

Aufarbeitung

customreaction
temperaturethe mixture was cooled to RT
custompurified completely by preparative HPLC (Method 10)
customDrying in an HV

Quellen und Nachweise

ORD-Eintrag: ord-aa3f242f2f644988857c1a2cfbe2db55
Quelldatensatz: uspto-grants-2014_08
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08796324B2

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