N-Methylethylamine → N-ethyl-N-methyl-2-{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}acetamide

HRID 230662

Reaktionsgleichung

Reaktionsgleichung von HRID 230662
[F:1][C:2]([F:23])([F:22])[C:3]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[N:5]([C:12]2[CH:17]=[CH:16][C:15]([CH2:18][C:19]([OH:21])=O)=[CH:14][CH:13]=2)[N:4]=1.[CH2:24]([NH:26][CH3:27])[CH3:25]>>[CH2:24]([N:26]([CH3:27])[C:19](=[O:21])[CH2:18][C:15]1[CH:14]=[CH:13][C:12]([N:5]2[C:6]3[CH2:7][CH2:8][CH2:9][CH2:10][C:11]=3[C:3]([C:2]([F:23])([F:22])[F:1])=[N:4]2)=[CH:17][CH:16]=1)[CH3:25]

Komponenten

3

Edukt 2

HCID 12219N-MethylethylamineHCID 50992931{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}acetic acid

Produkt 1

HCID 24827046N-ethyl-N-methyl-2-{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}acetamide

Versuchsvorschrift

The title compound was prepared from {4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}acetic acid and N-ethylmethylamine using a similar procedure to that described for Example 13, but purified by flash column chromatography eluting from 0-100% ethyl acetate in hexane.

Aufarbeitung

  1. custompurified by flash column chromatography
  2. washeluting from 0-100% ethyl acetate in hexane

Quellen und Nachweise

ORD-Eintrag
ord-fb37fa22775246bc8c185de260bcd0db
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07566735B2

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