Sodium Bicarbonate → 3-ethylsulfanyl-N-(4-trifluoromethoxyphenyl)picolinamide

HRID 713655

Reaktionsgleichung

Reaktionsgleichung von HRID 713655
[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:10]=[CH:9][C:7]([NH2:8])=[CH:6][CH:5]=1.[CH2:13]([S:15][C:16]1[C:17]([C:22](O)=[O:23])=[N:18][CH:19]=[CH:20][CH:21]=1)[CH3:14].CCN=C=NCCCN(C)C.Cl.C(=O)(O)[O-].[Na+]>C1C=CC2N(O)N=NC=2C=1.N1C=CC=CC=1>[CH2:13]([S:15][C:16]1[C:17]([C:22]([NH:8][C:7]2[CH:9]=[CH:10][C:4]([O:3][C:2]([F:11])([F:12])[F:1])=[CH:5][CH:6]=2)=[O:23])=[N:18][CH:19]=[CH:20][CH:21]=1)[CH3:14]

Komponenten

7

Versuchsvorschrift

A mixture of 0.35 g of 4-trifluoromethoxyaniline, 0.36 g of 3-ethylsulfanylpicolinic acid, 0.46 g of EDCI hydrochloride, 0.02 g of HOBt and 3 mL of pyridine was stirred at room temperature overnight. A saturated aqueous sodium bicarbonate solution was poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting solid was washed with hexane and dried to obtain 0.60 g of 3-ethylsulfanyl-N-(4-trifluoromethoxyphenyl)picolinamide (hereinafter, referred to as Compound of Present Invention 18).

Aufarbeitung

  1. extractionthe mixture was extracted with ethyl acetate
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. washthe resulting solid was washed with hexane
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-8bf246cef7684967ad24936a9495a887
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09185910B2

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