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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1370285Erstellt: 26. Oktober 2026

Ethanol → HCID 178436644, Verbindung

https://huagongshe.com/reaction/1370285

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt4-Chloro-5-(4-ethylphenoxy)pyrimidineHCID 22380481—
EduktHCID 178436643HCID 178436643—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 178436644HCID 17843664477%

Reaktionsschritte

Science, 230-440 mesh) (13×4 cm column bed) using ethyl acetate as the eluent for the first 1.2 L and then with 5% ethanol in ethyl acetate. The fractions that contained homogeneous product were spin evaporated in vacuo to give a syrup. The pure 5-(4-ethylphenoxy)-4-(trans-4-hydroxycyclohexylamino)pyrimidine was converted to the hydrochloride by the same procedure described in Example 4. The residue was triturated under ethyl acetate to give a white solid which was collected, washed with ethyl acetate and dried in vacuo to give 1.25 g (77% yield) of 5-(4-ethylphenoxy)-4-(trans-4-hydroxycyclohexylamino)pyrimidine hydrochloride as a white solid, mp 245-243° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06583148B1
Quelldatensatzuspto-grants-2003_06
ORD IDord-947d7ce97c5a47748fdadb301ac840c4
Quellennotizuspto-grants-2003_06