[C:1]([C-:3]([C:6]#[N:7])[C:4]#[N:5])#[N:2].[K+].S(=O)(=O)(O)O.[CH2:14]([NH:17][CH2:18][CH2:19][CH3:20])[CH2:15][CH3:16]>O.C(OCC)C>[NH2:2][C:1]([N:17]([CH2:18][CH2:19][CH3:20])[CH2:14][CH2:15][CH3:16])=[C:3]([C:6]#[N:7])[C:4]#[N:5]In the manner of Example VI, part C, 25 g of potassium tricyanomethanide in 75 ml of water and 100 ml of diethyl ether were treated with 19 g of concentrated sulfuric acid to give an ether solution of HN=C=C(CN)2. The ether solution was treated with 19.6 g of dipropylamine and the mixture allowed to stand for 1/2 hour. The ether was removed by distillation under reduced pressure and the residue heated to 150°. To the hot residue were added 500 ml of aqueous ethanol and the mixture was boiled vigorously for 15 minutes. The mixture was again concentrated and the residue heated at 150° for about 16 hours. The mixture was dissolved in aqueous ethanol, treated with activated charcoal and chilled for two days at about 5°. The separated solid was collected by filtration and dried to give 31 g of 3-amino-2-cyano-3-(dipropylamino)propenenitrile, m.p. 100°-105° from toluene. The ir and nmr spectra were consistent with the assigned structure.
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