Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1371454Erstellt: 25. Oktober 2026

1,4-Oxathiane → N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}thiomorpholine-4-carboxamide

https://huagongshe.com/reaction/1371454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-OxathianeHCID 27596—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Nitrophenyl [4-(3,4-dichlorobenzyl)morpholin-2-yl]methylcarbamateHCID 11539448—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}thiomorpholine-4-carboxamideHCID 17984668—

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

1,4-Thioxane (0.02 g) and N,N-diisopropylethylamine (0.04 ml) were added to a solution of Intermediate 10 (0.08 g) in dichloromethane (2 ml). The mixture was stirred at 23° C. for 16 h, and the solvent evaporated in vacuo. The residue was dissolved in dichloromethane (3 ml), and the solution shaken with polystyrene methyl isocyanate resin (Argonaut Technologies, 0.14 g, 1.45 mmol/g) for 2 h. The solution was drained from the resin, and the resin washed with dichloromethane (6 ml) and methanol (3 ml); the combined filtrate and washings were concentrated in vacuo. The residue was purified further by solid phase extraction (Isolute SCX sulphonic acid column), eluting with methanol followed by 10% 0.880 ammonia solution in methanol, to give the title compound as a pale yellow gum (0.065 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157457B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-01757b5b056844ad8f89f33a4e0f286d
Quellennotizuspto-grants-2007_01