2-Bromoethyl methyl ether → Ethyl [2-imino-3-(2-methoxyethyl)-2,3-dihydro-1,3-thiazol-4-yl]acetate hydrobromide

HRID 1037828Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1037828
[CH2:1]([O:3][C:4](=[O:12])[CH2:5][C:6]1[N:7]=[C:8]([NH2:11])[S:9][CH:10]=1)[CH3:2].[CH3:13][O:14][CH2:15][CH2:16][Br:17]>>[BrH:17].[NH:11]=[C:8]1[N:7]([CH2:16][CH2:15][O:14][CH3:13])[C:6]([CH2:5][C:4]([O:3][CH2:1][CH3:2])=[O:12])=[CH:10][S:9]1

Komponenten

3

Edukt 2

HCID 809722-Bromoethyl methyl etherHCID 1044544-Thiazoleacetic acid, 2-amino-, ethyl ester

Produkt 1

HCID 86618901Ethyl [2-imino-3-(2-methoxyethyl)-2,3-dihydro-1,3-thiazol-4-yl]acetate hydrobromideAusbeute 83 %

Versuchsvorschrift

A mixture of (2-aminothiazol-4-yl)acetic acid ethyl ester (18.6 g, 100 mmol) and 2-bromoethyl methyl ether (15.3 g, 110 mmol) were processed using the method described in Example 2A to afford 14.1 g (83%) of the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.14-1.28 (m, 3H) 3.24 (s, 3H) 3.54 (t, J=5 Hz, 2H) 3.91 (s, 2H) 4.04-4.25 (m, 4H) 6.92 (s, 1H) 9.50 (s, 1H); MS (DCI/NH3) m/z 231 (M+H)+.

Quellen und Nachweise

ORD-Eintrag
ord-415a1b66160847e28e6e5c14e4e43154
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08546583B2

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