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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 968539Erstellt: 24. Oktober 2026

Phenyl chloroformate → HCID 178488703, Verbindung

https://huagongshe.com/de/reaction/968539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenyl chloroformateHCID 15891—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Methoxy-7-(tetrahydro-pyran-4-yl)-benzothiazol-2-yl-amineHCID 22015735—
Edukt(4-Methoxy-7-phenyl-benzothiazol-2-yl)-carbamic acid benzyl esterHCID 86584926—
EduktHCID 178521615HCID 178521615—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178488703HCID 1784887037%

Reaktionsschritte

4-Methoxy-7-(tetrahydro-pyran-4-yl)-benzothiazol-2-ylamine (69 mg, 0.26 mmol) is first reacted with phenyl chloroformate as described for (4-methoxy-7-phenyl-benzothiazol-2-yl)-carbamic acid benzyl ester in WO01/97786 and then with N-ethyl-diisopropylamine (0.090 ml, 0.52 mmol) and (trans)-cyclohexane-1,4-diol (60 mg, 0.52 mmol) in dimethyl sulfoxide (10 ml) at 50° C. for 2 h. Then 100 ml dichoromethane are added, the mixture is extracted with saturated aqueous sodium carbonate and the organic phase is dried and evaporated. Flash-chromatographic purification (silica, eluting with dichloromethane/methanol) yielded the title compound as white solid (7% yield). MS: m/e=407(M+H+), mp 282-284° C. Following the general method of example 1 the compounds of examples 2 to 11 were prepared.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07304058B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-11fd3b0b8d58482a8356e58c8abe301d
Quellennotizuspto-grants-2007_12