Triethylamine → 2-{5-[({[6-Chloro-4-(trifluoromethyl)pyridin-2-yl]carbamoyl}amino)sulfonyl]-3-methyl-2-thienyl}ethyl acetate

HRID 1696771Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1696771
[CH3:1][C:2]1[CH:6]=[C:5]([S:7](=[O:10])(=[O:9])[NH2:8])[S:4][C:3]=1[CH2:11][CH2:12][O:13][C:14](=[O:16])[CH3:15].[C:17]1([O:23]C(Cl)=O)C=CC=CC=1.C(N(CC)CC)C.[Cl:34][C:35]1[N:40]=[C:39]([NH2:41])[CH:38]=[C:37]([C:42]([F:45])([F:44])[F:43])[CH:36]=1>C(#N)C>[C:14]([O:13][CH2:12][CH2:11][C:3]1[S:4][C:5]([S:7]([NH:8][C:17](=[O:23])[NH:41][C:39]2[CH:38]=[C:37]([C:42]([F:45])([F:43])[F:44])[CH:36]=[C:35]([Cl:34])[N:40]=2)(=[O:10])=[O:9])=[CH:6][C:2]=1[CH3:1])(=[O:16])[CH3:15]

Komponenten

6

Versuchsvorschrift

To a solution of 0.263 g acetic acid 2-(3-methyl-5-sulfamoyl-thiophen-2-yl)-ethyl ester in 5 ml acetonitrile was added 0.188 g phenylchloroformate and 0.252 g triethylamine at ° C. and the mixture was stirred at this temperature for 2 h. To the resulting suspension was added 0.196 g 6-chloro-4-trifluoromethyl-pyridin-2-ylamine and the mixture was heated to 60C for 18 h. The reaction mixture was partitioned between 10% citric acid and ethyl acetate. The phases were separated and the organic phase was washed with brine and evaporated. The residue was triturated with diethylether. The solid was collected by filtration to yield the title compound as white crystals. MS (ISN) M−H+=488.4

Aufarbeitung

  1. customThe reaction mixture was partitioned between 10% citric acid and ethyl acetate
  2. customThe phases were separated
  3. washthe organic phase was washed with brine
  4. customevaporated
  5. customThe residue was triturated with diethylether
  6. filtrationThe solid was collected by filtration

Quellen und Nachweise

ORD-Eintrag
ord-70053527550941f397a8f12ac9f19a24
Quelldatensatz
uspto-grants-2012_04
Patentnummer
US08163778B2

Notizen zur Reaktion

Wird geladen…