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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353739Erstellt: 25. Oktober 2026

Cyanamide → [4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][4-(1-pyrrolidinyl)phenyl]methanone

https://huagongshe.com/reaction/353739

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyanamideHCID 9864—
Edukt4-(Pyrrolidin-1-yl)phenacyl bromideHCID 3681785—
Edukt1-(4-Isothiocyanatophenyl)-4-methylpiperazineHCID 13718397—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelAcetonitrileHCID 6342—
Lösungsmitteltert-ButanolHCID 6386—
Produkt[4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][4-(1-pyrrolidinyl)phenyl]methanoneHCID 219589134%

Reaktionsschritte

tert-Butanol (4 mL) and then 1-(4-isothiocyanatophenyl)-4-methyl piperazine (of Example 1; 219 mg, 1 mmol) were added to a solution of cyanamide (44 mg, 1.05 mmol) in acetonitrile (5 mL). Potassium t-butoxide (1 M in tert-butanol; 1 mL, 1 mmol) was added and the solution was stirred for 30 min. 2-Bromo-1-[4-(1-pyrrolidinyl)phenyl]ethanone (257 mg, 1 mmol) (Lancaster) was added, and the solution was stirred at room temperature for 2 days. The yellow-brown solid was filtered off and washed with cold acetonitrile, water and then cold acetonitrile (weight of solid: 271 mg). A portion of this crude product (50 mg) was purified by chromatography (10% methanol/dichloromethane) to give [4-amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][4-(1-pyrrolidinyl)phenyl]methanone (18.5 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06756374B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-6b40e8cc083f4f0e890d9a34e6cb08eb
Quellennotizuspto-grants-2004_06