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Cyanamide → N,N'-dicyano-N"-[2-(5-methylimidazol-4-ylmethylthio)ethyl]guanidine

HRID 1702479
ノート
印刷プレビュー

反応式

HRID 1702479 の反応式
[Na].[N:2]#[C:3][NH2:4].[C:5]([NH:7][C:8](=[N:11][CH2:12][CH2:13][S:14][CH2:15][C:16]1[N:17]=[CH:18][NH:19][C:20]=1[CH3:21])SC)#[N:6]>C(O)C>[C:3]([NH:4][C:8]([NH:7][C:5]#[N:6])=[N:11][CH2:12][CH2:13][S:14][CH2:15][C:16]1[N:17]=[CH:18][NH:19][C:20]=1[CH3:21])#[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 9864CyanamideHCID 1036301-Cyano-2-methyl-3-(2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)isothioureaHCID 5360545Sodium

生成物 1

HCID 12918616N,N'-dicyano-N"-[2-(5-methylimidazol-4-ylmethylthio)ethyl]guanidine収率 49.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of sodium metal (1.01 g) in ethanol (120 ml) were added cyanamide (18.5 g) and N-cyano-S-methyl-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]isothiourea (10.76 g). The resulting mixture was heated under reflux for 1.5 hrs. After concentration under a reduced pressure, the residue was added to cold water (50 ml) and acidified (pH 4.5) with 10% HCl and cooled for 1 hr. in an ice bath. The precipitate was filtered, washed with water and dried. The resulting crude product (7.43 g) was recrystallized from C2H5OH-H2O (1:1) to give N,N'-dicyano-N"-[2-(5-methylimidazol-4-ylmethylthio)ethyl]guanidine (5.17 g).

後処理

  1. temperatureThe resulting mixture was heated
  2. temperatureunder reflux for 1.5 hrs
  3. concentrationAfter concentration under a reduced pressure
  4. additionthe residue was added to cold water (50 ml)
  5. temperaturecooled for 1 hr
  6. filtrationThe precipitate was filtered
  7. washwashed with water
  8. customdried
  9. customThe resulting crude product (7.43 g) was recrystallized from C2H5OH-H2O (1:1)

出典と根拠

ORDレコード
ord-c05a2444871f41fba6b7fac0cf1412bb
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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