Potassium Carbonate → HCID 178485057, compound

HRID 127319Notes

Reaction equation

HRID 127319 reaction equation
C(=O)([O-])[O-].[K+].[K+].[CH3:7][N:8]([CH2:10][C:11]1[O:15][C:14]([CH2:16][S:17][CH2:18][CH2:19][NH2:20])=[CH:13][CH:12]=1)[CH3:9].CS[C:23](=[N:27][CH3:28])[NH:24][C:25]#[N:26]>C(#N)C.[N+]([O-])([O-])=O.[Ag+]>[C:25]([N:24]=[C:23]([NH:27][CH3:28])[NH:20][CH2:19][CH2:18][S:17][CH2:16][C:14]1[O:15][C:11]([CH2:10][N:8]([CH3:7])[CH3:9])=[CH:12][CH:13]=1)#[N:26]

Participants

6

Procedure

To a stirred suspension of potassium carbonate (20.7 g) in a solution of 2-[[[5-(dimethylamino)methyl-2-furanyl]methyl]thio]ethanamine (10.7 g) and N-cyano-N'-methylcarbamimidothioic acid methyl ester (7.1 g) in acetonitrile (107 ml) at 70° was added a solution of silver nitrate (9.35 g) in acetonitrile (20 ml) during 1 hr. The mixture was stirred for 16 hr, the solid filtered and the filtrate evaporated to dryness. The residue was dissolved in ethyl acetate (250 ml). A portion of this (10.5 ml) was washed with water (6 ml), the ethyl acetate layer evaporated to give a solid which was crystallised from isoproplyacetate (1.75 ml) giving N"-cyano-N-[2-[[[5-(dimethylaminomethyl)-2-furanyl]methyl]thio]ethyl]-N'-methylguanidine (0.35 g) m.p. 79°-81.5°.

Workup

  1. filtrationthe solid filtered
  2. customthe filtrate evaporated to dryness
  3. dissolutionThe residue was dissolved in ethyl acetate (250 ml)
  4. washA portion of this (10.5 ml) was washed with water (6 ml)
  5. customthe ethyl acetate layer evaporated
  6. customto give a solid which
  7. customwas crystallised from isoproplyacetate (1.75 ml)

Sources & evidence

ORD record
ord-9a1243491290403bb31b13f85b1c8c1e
Source dataset
uspto-grants-1981_03
Patent number
US04255440

Reaction notes

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