HCID 176526843, Verbindung → HCID 178508737, Verbindung

HRID 1112535Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1112535
Cl.[NH:2]=[C:3]1[NH:7][C:6](=[NH:8])[CH2:5][S:4]1.[NH:9]=[C:10]1[C:18]2[CH2:17][CH2:16][CH2:15][CH2:14][C:13]=2[C:12](=N)[NH:11]1>CO>[NH:9]=[C:10]1[C:18]2[CH2:17][CH2:16][CH2:15][CH2:14][C:13]=2[C:12](=[C:5]2[S:4][C:3](=[NH:2])[NH:7][C:6]2=[NH:8])[NH:11]1

Komponenten

4

Edukt 2

HCID 176526843HCID 176526843, VerbindungHCID 178479111HCID 178479111, Verbindung

Produkt 1

HCID 178508737HCID 178508737, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A mixture of 6 parts of 2,4-diiminothiazolidine hydrochloride, 6 parts of 4,5,6,7-tetrahydro-1,3-diiminoisoindoline and 100 arts of anhydrous methyl alcohol was stirred and heated at reflux under an atmosphere of nitrogen for approximately 16 hours. The reaction was then cooled and filtered. The solid product collected by filtration was converted to the free base by treatment with a slight excess of a methyl alcohol solution of triethylamine and the product thus obtained was recrystallized frm acetic acid. The resultant acetate salt was treated with dilute ammonium hydroxide and the product isolated to obtain in the free-base form 1-imino-4,5,6,7-tetrahydro-3-(2,4-diimino-5-thiazolidinylidene)isoindoline as a greenish-brown powder melting at 215°-223° C. (dec).

Aufarbeitung

  1. temperatureheated
  2. temperatureat reflux under an atmosphere of nitrogen for approximately 16 hours
  3. temperatureThe reaction was then cooled
  4. filtrationfiltered
  5. filtrationThe solid product collected by filtration
  6. customthe product thus obtained
  7. customwas recrystallized frm acetic acid
  8. additionThe resultant acetate salt was treated with dilute ammonium hydroxide
  9. customthe product isolated

Quellen und Nachweise

ORD-Eintrag
ord-f2d8a4935a744c31a5f3e7d275b469b7
Quelldatensatz
uspto-grants-1978_10
Patentnummer
US04122261

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