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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1628233Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1-(Thiazol-4-yl)cyclopropanamine

https://huagongshe.com/reaction/1628233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBoron trifluoride etherateHCID 8000—
EduktSodium HydroxideHCID 14798—
Edukt4-CyanothiazoleHCID 15069—
EduktHCID 178418443HCID 178418443—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-(Thiazol-4-yl)cyclopropanamineHCID 5528567649,3%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

Thiazole-4-carbonitrile (1035 mg, 9397 μmol) was azeotroped with toluene. Et2O was added, and the clear solution was cooled to −70° C., followed by addition of titanium tetraisopropoxide (3025 μl, 10337 μmol), and ethylmagnesium bromide (6265 μl, 18795 μmol). The reaction mixture turned yellow. It remained yellow until about 15 min. The reaction was raised to RT, the solution changed into black. After 1 h., boron trifluoride diethyl etherate (2361 μl, 18795 μmol) was added and stirred for 1.5 hr. Then 1N HCl 27 mL was added, followed by 100 mL ether, 95 mL 10% NaOH. The reaction was extracted with Et2O×2 and 30% IPA/CHCl3×1. The organic layer was concentrated and purified with silica gel chromatography using 0-10% MeOH/DCM. 650 mg of product 14.2.B was obtained in 49% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08785468B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-ae043e8723ad458a9b60ddee57e3eb51
Quellennotizuspto-grants-2014_07