反应详情

温度

20 °C

A solution of 12.9 g of 10-acetamido-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one in 650 ml of 2N aqueous hydrochloric acid solution is heated to boiling for 2 hours, cooled and then concentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 80° C. 4 g (of the 14.8 g obtained in total) are dissolved in 250 ml of distilled water and the solution is stirred for 16 hours at a temperature in the region of 20° C. The crystals formed are separated out by filtration, washed successively with 25 ml of distilled water and 25 ml of methanol and then air-dried at a temperature in the region of 20° C. The product obtained (3.5 g) is stirred in suspension for 10 minutes in 100 ml of boiling methanol and, after cooling and storing for 1 hour at 5° C., is isolated by filtration, washed with 20 ml of chilled methanol and then dried under reduced pressure (1 mmHg; 0.13 kPa) at 100° C. 2.1 g of 10-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one hydrochloride are thus obtained, decomposing without melting at about 240° C. [N.M.R. spectrum: (200 MHz; DMSO d6 ; δ in ppm): 5.70 (broad s, 1H: CH--N+ --Cl-); 7.48 and 7.58 (2t, J=7.5 Hz, 1H each: --H7 and --H8); 7.72 and 8.76 (2s, 1H each: --H of the imidazole); 7.98 and 8.09 (2d, J=7.5 Hz, 1H each: --H6 and --H9); 9.47 (cplx, 3H: N+ H3Cl-); 12.80 (cplx, 1H: --NH--)].

1. temperaturecooled
2. concentrationconcentrated to dryness under reduced pressure (15 mmHg; 2 kPa) at 80° C
3. custom4 g (of the 14.8 g obtained in total)
4. customThe crystals formed
5. customare separated out by filtration
6. washwashed successively with 25 ml of distilled water and 25 ml of methanol
7. customair-dried at a temperature in the region of 20° C
8. customThe product obtained (3.5 g)
9. temperatureafter cooling
10. waitstoring for 1 hour at 5° C.
11. customis isolated by filtration
12. washwashed with 20 ml of chilled methanol
13. customdried under reduced pressure (1 mmHg; 0.13 kPa) at 100° C