2-(Chloromethyl)aniline hydrochloride → HCID 178488113, Verbindung

HRID 1586471Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1586471
[SH:1][C:2]1[NH:3][C:4]2[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:5]=2[N:6]=1.Cl.Cl[CH2:15][C:16]1[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=1[NH2:18]>C(O)(C)C>[CH3:12][O:11][C:9]1[CH:8]=[CH:7][C:5]2[NH:6][C:2]([S:1][CH2:15][C:16]3[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=3[NH2:18])=[N:3][C:4]=2[CH:10]=1

Komponenten

4

Versuchsvorschrift

The title compound was prepared by the method of Example 1 using 1.68 g (9.33 mMol) of 2-mercapto-5-methoxybenzimidazole instead of 2-mercaptobenzimidazole and 1.99 g (11.2 mMol) of 2-(chloromethyl)aniline hydrochloride instead of 2-(chloromethyl)-N,N-dimethylaniline in 250 ml of isopropyl alcohol. The basic extraction used 5% sodium hydroxide instead of sodium carbonate. Chromatography on silica gel, followed by crystallization from diethylether, gave 520 mg of pure title compound: m.p. 140-142° C. Anal. Calc'd. for C15H15N3OS: C, 63.14; H, 5.30; N,14.73; S, 11.23. Found: C, 63.44; H, 5.42; N, 14.43; S, 11.07.

Aufarbeitung

  1. extractionThe basic extraction
  2. customChromatography on silica gel, followed by crystallization from diethylether

Quellen und Nachweise

ORD-Eintrag
ord-86356c6eae19491ba06ec6719fe2c891
Quelldatensatz
uspto-grants-1999_08
Patentnummer
US05945425

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