1,2-Dichloroethane → 2-[3-(4-Chlorophenyl)-5-oxo-4-(3,3,3-trifluoropropyl)-4,5-dihydro-1H-1,2,4-triazol-1-yl]-N-{1-(2,3-dichlorophenyl)-2-[(ethylcarbamoyl)amino]ethyl}acetamide

HRID 2402845Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2402845
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([CH2:13][CH2:14][C:15]([F:18])([F:17])[F:16])[C:11](=[O:19])[N:10]([CH2:20][C:21]([OH:23])=O)[N:9]=2)=[CH:4][CH:3]=1.[CH2:24]([Cl:27])[CH2:25][Cl:26].[CH:28]1[CH:29]=[CH:30][C:31]2[N:36](O)N=[N:34][C:32]=2[CH:33]=1.[CH:38]([N:41]([CH2:45]C)C(C)C)(C)[CH3:39].CN(C=[O:51])C>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([CH2:13][CH2:14][C:15]([F:18])([F:17])[F:16])[C:11](=[O:19])[N:10]([CH2:20][C:21]([NH:34][CH:32]([C:33]3[CH:28]=[CH:29][CH:30]=[C:25]([Cl:26])[C:24]=3[Cl:27])[CH2:31][NH:36][C:45](=[O:51])[NH:41][CH2:38][CH3:39])=[O:23])[N:9]=2)=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

Of the compound from Example 177A, 145 mg (0.42 mmol), 143 mg (0.46 mmol) of the compound from Example 154A, 96 mg (0.50 mmol) of EDC, 67 mg (0.50 mmol) of HOBt and 87 μl (0.50 mmol) of N,N-diisopropylethylamine were stirred in 4.9 ml of DMF at RT for 1 h. The entire solution was purified by preparative HPLC [Method 20]. The product fraction was freed from the solvents on a rotary evaporator and the residue was dried in an HV. This gave 150 mg (58% of theory) of the title compound.

Aufarbeitung

  1. customThe entire solution was purified by preparative HPLC [Method 20]
  2. customThe product fraction was freed from the solvents on a rotary evaporator
  3. customthe residue was dried in an HV

Quellen und Nachweise

ORD-Eintrag
ord-115e22f14a84426fb245c2eda737f3f3
Quelldatensatz
uspto-grants-2014_08
Patentnummer
US08796324B2

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