Dichloromethane → HCID 14769542、化合物
反応式
[CH:1]([NH:3][C:4]1[S:8][N:7]=[C:6]([C:9]([O:11]C)=O)[N:5]=1)=[O:2].[CH3:13][S:14][CH2:15][S:16]([CH3:18])=[O:17].[H-].[Na+].C(Cl)Cl>CN(C)C=O>[CH:1]([NH:3][C:4]1[S:8][N:7]=[C:6]([C:9](=[O:11])[CH:15]([S:14][CH3:13])[S:16]([CH3:18])=[O:17])[N:5]=1)=[O:2]参加物
反応条件
- 温度
- 40 °C
実験手順
To a mixture of methyl 5-formamido-1,2,4-thiadiazole-3-carboxylate (9.2 g) and methyl methylthiomethyl sulfoxide (6.1 g) in N,N-dimethylformamide (100 ml) was added 50% sodium hydride (7.1 g) with cooling in an ice-bath. The mixture was stirred for an hour at ambient temperature and for an additional one hour at 40° C. After cooling to ambient temperature, methylene chloride (300 ml) was added to the reaction mixture, and the resulting precipitates were collected by filtration and washed with methylene chloride. The precipitates were added to a stirred mixture of hydrochloric acid (14.7 ml), ice-water (200 ml) and methylene chloride (200 ml). An insoluble material was filtered off and the methylene chloride layer was separated from the filtrate. The solution was dried over anhydrous magnesium sulfate, evaporated and the residue was triturated with diethyl ether to give the title compound (4.5 g), mp. 130° to 132° C.
後処理
- temperaturewith cooling in an ice-bath
- temperatureAfter cooling to ambient temperature
- customthe resulting precipitates
- filtrationwere collected by filtration
- washwashed with methylene chloride
- additionThe precipitates were added to a stirred mixture of hydrochloric acid (14.7 ml), ice-water (200 ml) and methylene chloride (200 ml)
- filtrationAn insoluble material was filtered off
- customthe methylene chloride layer was separated from the filtrate
- dry with materialThe solution was dried over anhydrous magnesium sulfate
- customevaporated
- customthe residue was triturated with diethyl ether
出典と根拠
- ORDレコード
- ord-fd540f6546c944d8bcd307f2cc754d4e
- 出典データセット
- uspto-grants-1986_04
- 特許番号
- US04585872
反応ノート
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