Reaktionsgleichung
[CH2:1]([O:3][C:4]([C:6]1[N:7]([S:12]([CH3:15])(=[O:14])=[O:13])[CH:8]=[C:9]([NH2:11])[CH:10]=1)=[O:5])[CH3:2].[F:16][C:17]1[C:24]([F:25])=[CH:23][CH:22]=[CH:21][C:18]=1[CH:19]=O.CC1C=CC(S(O)(=O)=O)=CC=1>C1C=CC=CC=1>[CH2:1]([O:3][C:4]([C:6]1[N:7]([S:12]([CH3:15])(=[O:14])=[O:13])[CH:8]=[C:9]([N:11]=[CH:19][C:18]2[CH:21]=[CH:22][CH:23]=[C:24]([F:25])[C:17]=2[F:16])[CH:10]=1)=[O:5])[CH3:2]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 4-amino-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid ethyl ester (2.1 g, 9.04 mmol) in anhydrous benzene (100 mL) was added 2,3-difluoro-benzaldehyde (1.29 g, 9.08 mmol) and catalytic amount of TsOH. The reaction mixture was heated under reflux in the presence of Dean-Stark trap for 24 hours. The solvent was then removed by evaporation and the residue was dried on the high vacuum pump for 16 hours for the next step use (2.9 g crude product). 1H NMR (500 MHz, DMSO-d6) δ8.99 (s, 1H), 7.85 (t, 1H), 7.75 (s, 1H), 7.58 (m, 2H), 7.32 (m, 1H), 4.32 (q, 2H), 3.90 (s, 3H), 2.51 (DMSO), 1.35 (t, 3H) ppm.
Aufarbeitung
- temperatureThe reaction mixture was heated
- temperatureunder reflux in the presence of Dean-Stark trap for 24 hours
- customThe solvent was then removed by evaporation
- dry with materialthe residue was dried on the high vacuum pump for 16 hours for the next step use (2.9 g crude product)
Quellen und Nachweise
- ORD-Eintrag
- ord-dc2863dd10c9432d85f32b65b99bf4e1
- Quelldatensatz
- uspto-grants-2008_01
- Patentnummer
- US07314885B2
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