تفاعل #75149
ord-469b644151a9415fbfd03bf85b206a76
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1درجة الحرارةThe reaction mixture is cooled
- 2أخرىthe layers are separated
- 3تجفيفThe 4-methyl-2-pentanone-phase is dried
- 4ترشيحfiltered
- 5أخرىevaporated
- 6أخرىThe residue is purified by column-chromatography over silica gel using
- 7workup.ADDITIONa mixture of trichloromethane and 5% of methanol as eluent
- 8أخرىThe pure fractions are collected
- 9أخرىthe eluent is evaporated
- 10أخرىThe residue is triturated in 4-methyl-2-pentanone
- 11ترشيحThe solid product is filtered off
- 12أخرىdried
الإجراء التجريبي
A mixture of 4.8 parts of 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one, 5.6 parts of 3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one hydrochloride, 7.4 parts of sodium carbonate and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. The reaction mixture is cooled, water is added and the layers are separated. The 4-methyl-2-pentanone-phase is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is triturated in 4-methyl-2-pentanone. The solid product is filtered off and dried, yielding 4.0 parts (50%) of 8-[3-(1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one; mp. 186° C.