Hydrochloric Acid → HCID 20535093、化合物
反応式
[NH2:1][C:2]1[N:7]2[O:8][C:9](=[O:11])[N:10]=[C:6]2[N:5]=[C:4]([N:12]([CH2:16][CH:17]=[CH2:18])[CH2:13][CH:14]=[CH2:15])[N:3]=1.[C:19](Cl)(=[O:22])[CH:20]=[CH2:21].Cl>O.C(Cl)Cl.C(N(CC)CC)C>[CH2:13]([N:12]([CH2:16][CH:17]=[CH2:18])[C:4]1[N:3]=[C:2]([NH:1][C:19](=[O:22])[CH:20]=[CH2:21])[N:7]2[O:8][C:9](=[O:11])[N:10]=[C:6]2[N:5]=1)[CH:14]=[CH2:15]参加物
実験手順
6.5 g. of 7-amino-5-diallylamino-2H-[1,2,4]oxadiazolo[2,3-a]-s-triazin-2-one are suspended in 120 ml. of methylene chloride and 8 ml. of triethylamine. 3 ml. of acrylyl chloride in 35 ml. of methylene chloride are added dropwise at 0° C. while stirring. The mixture is then stirred for 2 hours, diluted with 100 ml. of water and adjusted to pH 4 with 2-N hydrochloric acid. The two phases are separated and the aqueous phase is extracted with methylene chloride. The combined organic extracts are dried over sodium sulfate and evaporated to dryness under reduced pressure. The residue is chromatographed over silica gel using methylene chloride and methanol for the elution and the desired substance is recrystallized from methylene chloride and diethyl ether, there being obtained pure N-{5-diallylamino-2-oxo-2H-[1,2,4]oxadiazolo[2,3-a]-s-triazin-7-yl}acrylamide having a melting point of 157°-161° C.
後処理
- stirringThe mixture is then stirred for 2 hours
- additiondiluted with 100 ml
- customThe two phases are separated
- extractionthe aqueous phase is extracted with methylene chloride
- dry with materialThe combined organic extracts are dried over sodium sulfate
- customevaporated to dryness under reduced pressure
- customThe residue is chromatographed over silica gel
- washfor the elution
- customthe desired substance is recrystallized from methylene chloride and diethyl ether, there
出典と根拠
- ORDレコード
- ord-fc128774da9940c2a766ede28089fb46
- 出典データセット
- uspto-grants-1982_06
- 特許番号
- US04336380
反応ノート
読み込み中…