Reaktion #168944

Reaktionsgleichung

2-(6-isopropyl-1,3-dimethyl-1H-indol-5-yloxy)-4-methoxy-but-2-enenitrile

guanidine carbonate

sodium methoxide

HCl

→

5-(6-Isopropyl-1,3-dimethyl-1H-indol-5-yloxy)-pyrimidine-2,4-diamine

Lösungsmittel

ethanol

Diethyl ether

diethyl ether

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeformed
2. 2
   SonstigeThe solid that had formed
3. 3
   Filtrationwas collected by filtration
4. 4
   Waschenwashed with diethyl ether
5. 5
   Sonstigedried under vacuum at 45 C
6. 6
   Sonstigeto give 171 mg

Vorschrift

5-(6-Isopropyl-1,3-dimethyl-1H-indol-5-yloxy)-pyrimidine-2,4-diamine was prepared from 2-(6-isopropyl-1,3-dimethyl-1H-indol-5-yloxy)-4-methoxy-but-2-enenitrile by treatment with guanidine carbonate and sodium methoxide using the procedure of step 7 of Example 2 above. This material was dissolved in 2.5 ml absolute ethanol, and 820 ml of 1 N HCl in diethyl ether was added with stirring. Diethyl ether was added slowly until small crystals formed, and the solution was then placed in a −10 C freezer for 18 hours. The solid that had formed was collected by filtration, washed with diethyl ether, and dried under vacuum at 45 C. to give 171 mg. of the hydrochloride salt, Mp: 185.1° C.

Quelle