Acetonitrile → 5-Aziridin-1-yl-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-yhnethyl)-benzamide

HRID 380695Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 380695
[Cl:1][C:2]1[CH:21]=[CH:20][C:19]([NH:22][CH2:23][CH2:24]Cl)=[CH:18][C:3]=1[C:4]([NH:6][CH2:7][C:8]12[CH2:17][CH:12]3[CH2:13][CH:14]([CH2:16][CH:10]([CH2:11]3)[CH2:9]1)[CH2:15]2)=[O:5].C(=O)([O-])[O-].[Cs+].[Cs+].C(#N)C>O>[N:22]1([C:19]2[CH:20]=[CH:21][C:2]([Cl:1])=[C:3]([CH:18]=2)[C:4]([NH:6][CH2:7][C:8]23[CH2:17][CH:12]4[CH2:13][CH:14]([CH2:16][CH:10]([CH2:11]4)[CH2:9]2)[CH2:15]3)=[O:5])[CH2:23][CH2:24]1

Komponenten

5

Edukt 3

HCID 6342AcetonitrileHCID 10796Cesium carbonateHCID 114176532-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)benzamide

Produkt 1

HCID 206700525-Aziridin-1-yl-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-yhnethyl)-benzamideAusbeute 17 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

2-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide (0.15 g), cesium carbonate (0.192 g) and acetonitrile (3 ml) were combined and heated in a sealed tube at 100° C. for 24 hours. The cooled reaction mixture was poured into water (50 ml) and the product extracted into ethyl acetate, dried over magnesium sulphate, filtered and concentrated under reduced pressure. The crude product was purified by NPHPLC eluting with 0-5% ethanol in dichloromethane to give the title compound as a white solid (0.023 g).

Aufarbeitung

  1. customThe cooled reaction mixture
  2. extractionthe product extracted into ethyl acetate
  3. dry with materialdried over magnesium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe crude product was purified by NPHPLC
  7. washeluting with 0-5% ethanol in dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-1059c17a3f404d3fa82c7c817e95c779
Quelldatensatz
uspto-grants-2001_10
Patentnummer
US06303659B2

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