反应 #416198
ord-2e425d794f7d46e083784e8fc07aa977
反应方程式
反应物
试剂
反应条件
后处理
- 1其他the solution which formed
- 2温度was cooled
- 3其他The crude, semisolid material which separated
- 4萃取the aqueous mother liquors were extracted with additional portions of ether
- 5浓缩The combined ethereal extracts were concentrated to 500 ml
- 6workup.ADDITIONand treated, under an atmosphere of nitrogen and with vigorous stirring, with 50 ml
- 7过滤The resulting precipitate was filtered off
- 8洗涤washed with ether and C (dec)
- 9干燥1N hydrochloric acid, and dried in vacuo at 100°
实验过程
A mixture of 24.6 g of N-aminoiminodibenzyl (5-amino-10,11-dihydro-5H-dibenz[b,f]azepine) and 14.8 g of 4-piperidone hydrochloride in 250 ml. ethanol was heated on a steam bath for 15 minutes 1,2,3,4,4cooled; 8,9,14a-octahydropyridoof 20 g. indoloconcentrated sulfuric acid in 250 ml. ethanol was added. The resulting mixture was reheated on the steam bath for an additional 40 minutes; the solution which formed was cooled, basified with ammonia, and diluted with 1 liter of water. The crude, semisolid material which separated was taken up in ether, and the aqueous mother liquors were extracted with additional portions of ether. The combined ethereal extracts were concentrated to 500 ml. and treated, under an atmosphere of nitrogen and with vigorous stirring, with 50 ml. of 5N hydrochloric acid. The resulting precipitate was filtered off, washed with ether and C (dec). 1N hydrochloric acid, and dried in vacuo at 100° to yield 1,2,3,8,9-hexahydropyrido[4',3':2,3]=indolo[1,7ab][1]benzazepine hydrochloride, m.p. 309°, a salt only very slightly soluble in water. Dissolving the above salt in aqueous acetic acid, basifying with ammonia, filtering off the crude product and recrystallizing it from benzene regenerated the free 1,2,3,4,8,9-hexahydropyrido[4',3':2,3]indolo[1,7-ab][1]benzazepine, m.p. 134°-136° C.