反応式
Br.[CH3:2][NH:3][C:4]1[CH:5]=[C:6]([CH:11]=[CH:12][CH:13]=1)[C:7](=O)[CH2:8]Br.[C:14]([NH:17][C:18]([NH2:20])=[S:19])(=[NH:16])[NH2:15]>C(O)C>[NH:17]([C:18]1[S:19][CH:8]=[C:7]([C:6]2[CH:11]=[CH:12][CH:13]=[C:4]([NH:3][CH3:2])[CH:5]=2)[N:20]=1)[C:14]([NH2:16])=[NH:15]参加物
4
実験手順
A mixture of 20 gm of 3-methylamino phenacyl bromide hydrobromide, 7.65 gm of amidinothiourea and 100 ml of ethanol was refluxed for 4 hours, and then cooled to room temperature. The dihydrobromide which separated out was filtered off, dissolved in water, and the solution was made alkaline with 10% sodium hydroxide. The free base was collected and dried, yielding 11.5 gm of the title compound, m.p. 198°-200° C.
後処理
- temperaturewas refluxed for 4 hours
- customThe dihydrobromide which separated out
- filtrationwas filtered off
- dissolutiondissolved in water
- customThe free base was collected
- customdried
出典と根拠
- ORDレコード
- ord-5c9fdc1750b64781aef4ae66f6302d9f
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04548944
関連ノート
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