1-Propanol → Propyl 3-amino-1H-furo[3,2-c]pyrazole-5-carboxylate
反応式
[C:1]([C:3]1[O:7][C:6]([C:8]([O:10][CH3:11])=[O:9])=[CH:5][C:4]=1[NH:12][N:13]=C(C1C=CC=CC=1)C1C=CC=CC=1)#[N:2].S(=O)(=O)(O)O.[CH2:32](O)[CH2:33]C>>[NH2:2][C:1]1[C:3]2[O:7][C:6]([C:8]([O:10][CH2:11][CH2:32][CH3:33])=[O:9])=[CH:5][C:4]=2[NH:12][N:13]=1参加物
4
実験手順
To a solution of 56.01 g (0.1624 mol) of methyl 5-cyano-4-[2-(diphenylmethylene)hydrazino]-2-furoate in 1.12 L of n-propanol was slowly added 115 mL (2.1 mol) of 98% sulfuric acid. The resulting mixture was refluxed for 2 hours obtaining a clear brown solution. The reaction mass was concentrated under reduced pressure to a small volume, cooled to 0/+4° C. and slowly diluted with 1.1 L of 25% trisodium citrate dihydrate solution over a period of 90 min. under efficient stirring. The mixture (pH=4) was extracted three times with 600 mL of cyclohexane. The organic extracts were discarded while the aqueous layer was cooled to 0/+4° C. and brought to pH 6-7 by carefully adding 1 L of 10% aqueous sodium bicarbonate and, finally, 82 mL of N-methylmorpholine. The resulting suspension was aged for 4 hours at 0/+2° C. and then filtered and washed thoroughly with water affording, after drying, 21.35 g of product as light brown solid.