Ethanolamine → N-(2-Hydroxy-ethyl)-3-{4-[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonamide

HRID 1928407Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1928407
[CH2:1]([CH2:3][NH2:4])[OH:2].C(N(CC)CC)C.Cl.[F:13][C:14]([F:48])([F:47])[C:15]1[CH:20]=[C:19]([C:21]2[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:23][CH:22]=2)[N:18]=[C:17]([C:31]2[CH:36]=[CH:35][N:34]=[C:33]([C:37]3[CH:38]=[C:39]([S:43](Cl)(=[O:45])=[O:44])[CH:40]=[CH:41][CH:42]=3)[CH:32]=2)[N:16]=1>C1COCC1>[OH:2][CH2:1][CH2:3][NH:4][S:43]([C:39]1[CH:40]=[CH:41][CH:42]=[C:37]([C:33]2[CH:32]=[C:31]([C:17]3[N:16]=[C:15]([C:14]([F:13])([F:47])[F:48])[CH:20]=[C:19]([C:21]4[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:28])[F:29])=[CH:23][CH:22]=4)[N:18]=3)[CH:36]=[CH:35][N:34]=2)[CH:38]=1)(=[O:44])=[O:45]

Komponenten

5

Versuchsvorschrift

To a cooled (ice-water bath) and stirred mixture of ethanolamine (0.066 g, 1.08 mmol), triethylamine (0.11 ml, 0.76 mmol) and THF (2 ml) was added drop wise a solution of 3-{4-[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonyl chloride hydrochloride (example I.1) (0.21 g, 0.36 mmol) in THF (3 ml). The mixture was allowed to stir at room temperature for 16 h. Purification of the reaction mixture by flash chromatography on silica gel (ethyl acetate/hexane) and crystallization (diethyl ether/hexane) yielded the title compound as a white solid (0.156 g, 76%). MS (ISP) 569.2 [(M+H)+]; mp 192.5° C.

Aufarbeitung

  1. stirringto stir at room temperature for 16 h
  2. customPurification of the reaction mixture by flash chromatography
  3. customon silica gel (ethyl acetate/hexane) and crystallization (diethyl ether/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-fcbb34c9e66f47a8b284bd7334b1012c
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08183262B2

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