反応式
[Br:1][CH2:2][C:3]([C:5]1[S:6][CH:7]=[CH:8][CH:9]=1)=[O:4].[CH3:10][C:11]1[S:15][C:14]([NH2:16])=[N:13][CH:12]=1>C(#N)C>[BrH:1].[NH:16]=[C:14]1[N:13]([CH2:2][C:3]([C:5]2[S:6][CH:7]=[CH:8][CH:9]=2)=[O:4])[CH:12]=[C:11]([CH3:10])[S:15]1参加物
4
実験手順
A mixture of 51 parts of 2-bromo-1-(2-thienyl)ethanone, 28.5 parts of 5-methyl-2-thiazolamine and 240 parts of acetonitrile was stirred for 1 hour while heating on a waterbath. After cooling, the precipitate was filtered off, washed with ethanol and dried in vacuo, yielding 54 parts of 2-(2,3-dihydro-2-imino-5-methyl-3-thiazolyl)-1-(2-thienyl)ethanone hydrobromide; mp. 207.5°-208° C. (interm. 56).
後処理
- temperaturewhile heating on a waterbath
- temperatureAfter cooling
- filtrationthe precipitate was filtered off
- washwashed with ethanol
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-ada5bbdbe62d4290905705d5d577da87
- 出典データセット
- uspto-grants-1993_05
- 特許番号
- US05212192
関連ノート
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