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HRID 52716Erstellt: 24. Oktober 2026

2-(N,N-Diethylamino)-4-(hydroxymethyl)thiazole → N-((2-(N,N-Diethylamino)-4-thiazolyl)methoxycarbonyl)valine Methyl Ester

https://huagongshe.com/de/reaction/52716

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(N,N-Diethylamino)-4-(hydroxymethyl)thiazoleHCID 18758970—
Edukta-Isocyanato-valine methyl esterHCID 22845662—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-((2-(N,N-Diethylamino)-4-thiazolyl)methoxycarbonyl)valine Methyl EsterHCID 5450233882%

Reaktionsschritte

A solution of 5.11 mmol of α-isocyanato-valine methyl ester in 10 ml of dichloromethane was treated with 0.864 g (4.65 mmol) of 2-(N,N-diethylamino)-4-(hydroxymethyl)thiazole and 0.46 mmol of 4-dimethylaminopyridine. The resulting solution was stirred at ambient temperature for 16 h, after which it was diluted with 200 ml of chloroform, washed successively with 10% citric acid, aqueous NaHCO3, and saturated brine. After drying over Na2SO4, the solvent was removed in vacuo, and the residue was chromatographed on silica gel using 1-2% methanol in chloroform to provide 1.31 g (82%) of the desired compound, Rf 0.51 (4% methanol in chloroform) as an oil. 1H NMR (CDCl3) δ0.89 (d, J=7 Hz, 3H), 0.96 (d, J=7 Hz, 3H), 1.24 (t, J=7 Hz, 6H), 2.15 (m, 1H), 3.51 (q, J=7 Hz, 4H), 3.74 (s, 3H), 4.29 (dd, J=8, 4 Hz, 1H), 5.03 (s, 2H), 5.34 (br d, J=8 Hz, 1H), 6.42 (s, 1H). Mass spectrum: (M+H)+ =344.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616720
Quelldatensatzuspto-grants-1997_04
ORD IDord-626a00d81aa445ff8f01adeee3e42e4c
Quellennotizuspto-grants-1997_04