Methylamine → HCID 178484998, compound

HRID 1287189Notes

Reaction equation

HRID 1287189 reaction equation
[CH3:1][NH2:2].[C:3]([NH:5][C:6](=[N:9][CH2:10][CH2:11][S:12][CH2:13][C:14]1[N:15]=[CH:16][NH:17][C:18]=1[CH3:19])SC)#[N:4]>C(O)C>[C:3]([NH:5][C:6]([NH:2][CH3:1])=[N:9][CH2:10][CH2:11][S:12][CH2:13][C:14]1[N:15]=[CH:16][NH:17][C:18]=1[CH3:19])#[N:4]

Participants

4

Procedure

A solution of methylamine in ethanol (33%, 75 ml) was added to a solution of N-cyano-N'-[2-((5-methyl-4-imidazolyl)methylthio)ethyl]-S-methylisothiourea (10.1 g) in ethanol (30 ml). The reaction mixture was set aside at room temperature for 2.5 hours. Following concentration under reduced pressure, the residue was recrystallised twice from isopropyl alcohol/petroleum ether, affording N-cyano-N'-methyl-N"-[2-((5-methyl-4-imidazolyl)methylthio)ethyl]guanidine, m.p. 141°-143°.

Workup

  1. concentrationconcentration under reduced pressure
  2. customthe residue was recrystallised twice from isopropyl alcohol/petroleum ether

Sources & evidence

ORD record
ord-f1cf6cea3b9842788caac0f3048cd3f6
Source dataset
uspto-grants-1976_10
Patent number
US03984293

Reaction notes

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