Methanol → HCID 178491901, Verbindung

HRID 370118Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 370118
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C:9](=[O:35])[C:10]2[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([O:17][CH3:18])[C:11]=2[NH:19][C:20]([C:22]2[S:23][CH:24]=[C:25]([CH2:28][N:29]3[CH:33]=[CH:32][N:31]=[C:30]3[NH2:34])[C:26]=2[Cl:27])=[O:21])=[N:6][CH:7]=1.S(=O)(=O)(O)O.ClN1[C:46](=[O:47])CCC1=O.[OH2:49].[CH3:50]O>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C:9](=[O:35])[C:10]2[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([O:17][CH3:18])[C:11]=2[NH:19][C:20]([C:22]2[S:23][CH:24]=[C:25]([CH2:28][N:29]3[C@H:33]([O:47][CH3:46])[C@H:32]([O:49][CH3:50])[NH:31][C:30]3=[NH:34])[C:26]=2[Cl:27])=[O:21])=[N:6][CH:7]=1

Komponenten

6

Versuchsvorschrift

N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide (0.053 g, 0.96 mmol) and sulfuric acid (0.10 g, 1.06 mmol) in methanol (10 mL) was added N-chlorosuccinimide (0.192 g, 1.43 mmol). After stirring at ambient temperature for 6 hours, the reaction was poured into water and extracted with ethyl acetate. The ethyl acetate extract was dried over sodium sulfate, concentrated in vacuo, and purified by flash chromatography on silica gel to give 0.33 g of N-(5-chloropyridin-2-yl)-2-[((4-((cis4,5-dimethoxy-2-iminotetrahydroimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide; NMR (CDCl3) 9.0 (d, 2), 8.3 (d, 1), 8.1 (d, 1), 7.7 (dd, 1), 7.5 (s, 1), 7.3 (d, 1), 7.1 (d, 1), 6.0 (brs, 1), 4.8 (m, 2), 4.6 (d, 1), 4.3 (d, 1), 3.9 (s, 3), 3.4 (s, 3), 3.3 (s, 3) ppm.

Aufarbeitung

  1. extractionextracted with ethyl acetate
  2. extractionThe ethyl acetate extract
  3. dry with materialwas dried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. custompurified by flash chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-505de881d1ec4333bd0bfb2d851b1c3a
Quelldatensatz
uspto-grants-2000_10
Patentnummer
US06140351

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