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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 558549Erstellt: 25. Oktober 2026

Iodine chloride → HCID 67000825, Verbindung

https://huagongshe.com/reaction/558549

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodine chlorideHCID 24640—
EduktSodium AcetateHCID 517045—
Edukt5-(4-Chlorophenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidineHCID 843838—
Edukt1-(4-Chlorophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 2773832—
EduktHCID 178418806HCID 178418806—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 67000825HCID 6700082598%

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

A mixture of commercially available 1-(4-chlorophenyl)-4,4,4-trifluoro-1,3-butanedione (8.65 g, 34.52 mmol) and commercially available 3-aminopyrazole (2.87 g, 34.52 mmol) in acetic acid (70 mL) was refluxed for 3 h (intermediate 5-(4-chloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine). Cooled to 23° C., added sodium acetate (3.54 g, 43.2 mmol) and a solution of iodine monochloride (2.11 mL, 41.4 mmol) in acetic acid (12 mL) was added dropwise, whereupon the reaction mixture solidified 2 min after complete addition. Added acetic acid (50 mL) and the mixture was stirred at 23° C. for additional 1 h. Diluted slowly with water (up to 400 mL), stirred at 23° C. for 30 min, the precipitate was filtered off, washed with water and dried in air at 50° C. to give a yellow solid, which was dissolved in EtOAc, washed with sat. NaHCO3-sol. and sat. Na2SO3-sol. and brine, dried over Na2SO4. Removal of the solvent in vacuum gave 5-(4-chloro-phenyl)-3-iodo-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine as a yellow solid (14.30 g, 98%). MS (EI) 422.9 [(M)+] and 425.0 [(M+2)+]; mp 155° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063048B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-c61b99acb60c43a78974f1c74c816e1f
Quellennotizuspto-grants-2011_11