Sodium hydride → 2-[2-(2,2,2-Trifluoroethyl)guanidino]-6-(3-aminopropylthio)pyrazine

HRID 1902327

反応式

HRID 1902327 の反応式
[H-].[Na+].Cl.[NH2:4][CH2:5][CH2:6][CH2:7][SH:8].[F:9][C:10]([F:24])([F:23])[CH2:11][N:12]=[C:13]([NH2:22])[NH:14][C:15]1[CH:20]=[N:19][CH:18]=[C:17](Cl)[N:16]=1>C(O)C>[F:24][C:10]([F:9])([F:23])[CH2:11][N:12]=[C:13]([NH2:22])[NH:14][C:15]1[CH:20]=[N:19][CH:18]=[C:17]([S:8][CH2:7][CH2:6][CH2:5][NH2:4])[N:16]=1

参加物

5

実験手順

Sodium hydride (50% w/w dispersion in oil; 0.57 g.) was added to ethanol (10 ml.) portionwise. To the resulting solution was added 3-aminopropanethiol hydrochloride (0.75 g.) and the mixture stirred at room temperature. 2-[2-(2,2,2-Trifluoroethyl)guanidino-6-chloropyrazine (0.5 g.) was added in one portion and the mixture heated under reflux on the steam bath overnight. The mixture was cooled, evaporated, water (10 ml.) added and the mixture extracted with ethyl acetate. The extracts were dried over magnesium sulphate, filtered and evaporated to yield an oil, which was chromatographed eluting with methanol/methylene chloride/ammonia 10:40:1 v/v/v yield 2-[2-(2,2,2-trifluoroethyl)guanidino]-6-(3-aminopropylthio)pyrazine as a pale yellow solid (0.39 g.) which was used without further purification.

後処理

  1. temperaturethe mixture heated
  2. temperatureunder reflux on the steam bath overnight
  3. temperatureThe mixture was cooled
  4. customevaporated
  5. additionwater (10 ml.) added
  6. extractionthe mixture extracted with ethyl acetate
  7. dry with materialThe extracts were dried over magnesium sulphate
  8. filtrationfiltered
  9. customevaporated
  10. customto yield an oil, which
  11. customwas chromatographed
  12. washeluting with methanol/methylene chloride/ammonia 10:40:1 v/v/v

出典と根拠

ORDレコード
ord-61af6b0cb2a1404ab95b97a313547a58
出典データセット
uspto-grants-1982_12
特許番号
US04362728

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