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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 418313Erstellt: 25. Oktober 2026

Hydrochloric Acid → 3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carboxylic acid [4-di-methylamino-4-(3-fluorophenyl)cyclohexyl]amide hydrochloride

https://huagongshe.com/reaction/418313

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktChlorotrimethylsilaneHCID 6397—
EduktDiisopropyl EtherHCID 7914—
Edukt4-Isoxazolecarboxylic acid, 3-(2,6-dichlorophenyl)-5-methyl-HCID 77521—
Edukt3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amideHCID 11691670—
Edukt1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamineHCID 57904199—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDiethyl ether methanolHCID 21864698—
Produkt3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carboxylic acid [4-di-methylamino-4-(3-fluorophenyl)cyclohexyl]amide hydrochlorideHCID 66651083—

Reaktionsschritte

As described for Example 120, 700 mg of a cis-trans mixture of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine were reacted with 810 mg 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylic acid (1 molar equivalent) and the crude product (1.86 g) was isolated. The main fraction, obtained after column chromatography on silica gel (3.0×19 cm) with 175 ml diethyl ether followed by 250 ml diethyl ether/methanol (V:V=2:1), 250 ml diethyl ether/methanol (V:V=1:1) and 100 ml methanol, of 950 mg was dissolved in 25 ml 2-butanone and 25 ml ethyl acetate and converted into the corresponding hydrochloride of the non-polar diastereoisomer of 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide by adding 35 μl water, 246 μl chlorotrimethylsilane and 25 ml diisopropylether (263 mg of white solid, Mp. 248-250° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093272B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-2bd0baf0b472493a8e8581b51adcf54d
Quellennotizuspto-grants-2012_01