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Sodium Sulfate → HCID 178485068、化合物

HRID 1702474
ノート
印刷プレビュー

反応式

HRID 1702474 の反応式
[C:1]([NH:3][C:4]([NH:6][CH3:7])=S)#[N:2].[CH3:8][C:9]1[NH:13][CH:12]=[N:11][C:10]=1[CH2:14][S:15][CH2:16][CH2:17][NH2:18].S([O-])([O-])(=O)=O.[Na+].[Na+]>CC#N>[C:1]([N:3]=[C:4]([NH:18][CH2:17][CH2:16][S:15][CH2:14][C:10]1[N:11]=[CH:12][NH:13][C:9]=1[CH3:8])[NH:6][CH3:7])#[N:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24436Sodium SulfateHCID 6655684-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 27241251-Cyano-3-methylthiourea

生成物 1

HCID 178485068HCID 178485068、化合物収率 7.6%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

A suspension of N-cyano-N'-methylthiourea (DBU salt) (0.534 g), 2-(5-methylimidazol-4-ylmethylthio)ethylamine (1.03 g), HgO (0.868 g) and anhydrous sodium sulfate (2 g) in CH3CN (20 ml) was heated under reflux for 20 hrs. with vigorous stirring. The hot reaction mixture was filtered and the filtrate was dried up and subjected to chromatography on SiO2 [eluant: CH3CN-CH3OH (4:1)]. The resulting crude product was purified by preparative thin layer chromatography [SiO2, AcOEt--MeOH--28% aq. NH3 (10:1:1)] and recrystallized from CH3CN to give N"-cyano-N-methyl-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]-guanidine (38.4 mg). Yield 7.6%, m.p. 136°-138° C.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 20 hrs
  3. filtrationThe hot reaction mixture was filtered
  4. customthe filtrate was dried up
  5. customThe resulting crude product was purified by preparative thin layer chromatography [SiO2, AcOEt--MeOH--28% aq. NH3 (10:1:1)]
  6. customrecrystallized from CH3CN

出典と根拠

ORDレコード
ord-610ef137ae304b709590dc3c90c07b08
出典データセット
uspto-grants-1983_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04381395

反応ノート

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