反応式
CN(C)C=O.Cl.[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([NH:16][C:17]2[CH2:22][CH2:21][CH2:20][C:19](=[O:23])[CH:18]=2)=[C:12]([CH:15]=1)[C:13]#[N:14].O=C1CCCC(NC2C=CC=CC=2C#N)=C1.C([O-])([O-])=O.[K+].[K+]>C1(C)C=CC=CC=1>[NH2:14][C:13]1[C:12]2[C:11]([N:16]=[C:17]3[C:18]=1[C:19](=[O:23])[CH2:20][CH2:21][CH2:22]3)=[CH:10][CH:9]=[C:8]([Cl:7])[CH:15]=2参加物
実験手順
In 5 liters of toluene were combined 200 ml of dimethylformamide, 180.71 g of 5-chloro-2-(3-oxocyclohexen-1-yl)aminobenzonitrile hydrochloride prepared in the same manner as the compounds of Examples 1 and 2, 176 g (2 eq) of milled K2CO3 and 3 g of cuprous chloride (CuCl). After 6 hours of reflux 3 g more of CuCl was added. After 12 hours of reflux 3 g more of CuCl was added. After overnight reflux the reaction mixture was evaporated and the residue extracted with dichloromethane via a Soxhlet extraction apparatus for 12 hours. The dichloromethane solution was evaporated to a solid. The solid was suspended in water and H2SO4 was added. The resultant salt which precipitated out was filtered and made basic with 10% NaOH. The solid was filtered and recrystallized twice from isopropanol/toluene to yield 6.84 g (4%) of a solid, melting point over 260° C.
後処理
- temperatureAfter overnight reflux the reaction mixture
- customwas evaporated
- extractionthe residue extracted with dichloromethane via a Soxhlet extraction apparatus for 12 hours
- customThe dichloromethane solution was evaporated to a solid
- additionH2SO4 was added
- customThe resultant salt which precipitated out
- filtrationwas filtered
- filtrationThe solid was filtered
- customrecrystallized twice from isopropanol/toluene
出典と根拠
- ORDレコード
- ord-967cb771ab304006a9c67c268998579c
- 出典データセット
- uspto-grants-1987_09
- 特許番号
- US04695573
関連ノート
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