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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390704Erstellt: 23. Oktober 2026

Diphosgene → N-(3-fluorobenzyl)-N-methyl-N'-(5-methyl-1,3-thiazol-2-yl)urea

https://huagongshe.com/de/reaction/390704

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphosgeneHCID 10426—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Amino-5-methylthiazoleHCID 351770—
EduktBenzenemethanamine, 3-fluoro-N-methyl-HCID 457577—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(3-fluorobenzyl)-N-methyl-N'-(5-methyl-1,3-thiazol-2-yl)ureaHCID 86631925—

Reaktionsschritte

5-Methylthiazol-2-amine (571 mg, 5.00 mmol) was dissolved into dichloromethane (30 mL) and cooled to near −45° C. Diphosgene (360 μL, 3.0 mmol) was added rapidly over a second or two, and the mixture was stirred for 5 minutes before diisopropylethylamine (1.74 mL, 10 mmol) was added. The solution was stirred for another 30 minutes, 3-fluorobenzyl-methylamine (1.03 mL, 7.5 mmol) was added, and after another couple of minutes, the cold bath was removed. When the reaction solution had warmed to near room temperature, it was quenched with 1 M aqueous potassium phosphate monobasic (15 mL). The aqueous phase was separated and back-extracted with dichloromethane, and the combined organic phases were washed with more 1 M aqueous KH2PO4 (5 mL). The aqueous phase was separated and back-extracted with dichloromethane. The combined organic phases were dried (sodium sulfate), concentrated, and chromatographed on acidic alumina (ethyl acetate/hexanes) to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383657B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-cbf1c44c12704b57a62b7916538e7867
Quellennotizuspto-grants-2013_02