Water → HCID 57069684, Verbindung

HRID 2231977Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2231977
[Cl:1][C:2]1[N:9]=[C:8](Cl)[CH:7]=[C:6]([CH3:11])[C:3]=1[C:4]#[N:5].NCCNC(=O)[CH:17]([C:19]1[CH:24]=[C:23]([C:25]([CH3:28])([CH3:27])[CH3:26])[C:22]([OH:29])=[C:21]([C:30]([CH3:33])([CH3:32])[CH3:31])[CH:20]=1)[CH3:18].C([N:37](CC)CC)C.O.C[N:44]1[CH2:48][CH2:47]C[C:45]1=[O:49]>C1(C)C=CC=CC=1>[C:30]([C:21]1[CH:20]=[C:19]([CH2:17][CH2:18][C:45]([NH:44][CH2:48][CH2:47][NH:37][C:8]2[CH:7]=[C:6]([CH3:11])[C:3]([C:4]#[N:5])=[C:2]([Cl:1])[N:9]=2)=[O:49])[CH:24]=[C:23]([C:25]([CH3:28])([CH3:26])[CH3:27])[C:22]=1[OH:29])([CH3:33])([CH3:32])[CH3:31]

Komponenten

7

Versuchsvorschrift

18.7 g of 2,6-dichloro-4-methylnicotinonitrile and 32 g of 3,5-di-tert-butyl-4-hydroxyphenylpropionic acid 2-aminoethylamide are reacted with 10.1 g of triethylamine in 0.2 l of N-methylpyrrolidone at 50° C. for 8 hours, after which 1 l of water and 0.4 l of toluene are added, the toluene phase is separated off, dried and filtered over active carbon, and the filtrate is evaporated down. The residue is dissolved in 100 ml of hot ethanol, and 1 l of petroleum ether is slowly added to the solution. The mixture is cooled, and the precipitate is filtered off under suction and dried to give a product of melting point 162°-165° C.

Aufarbeitung

  1. customthe toluene phase is separated off
  2. customdried
  3. filtrationfiltered over active carbon
  4. customthe filtrate is evaporated down
  5. dissolutionThe residue is dissolved in 100 ml of hot ethanol
  6. addition1 l of petroleum ether is slowly added to the solution
  7. temperatureThe mixture is cooled
  8. filtrationthe precipitate is filtered off under suction
  9. customdried
  10. customto give a product of melting point 162°-165° C.

Quellen und Nachweise

ORD-Eintrag
ord-23c2844a1e964804a3e1820609c83d29
Quelldatensatz
uspto-grants-1988_11
Patentnummer
US04785107

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