Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH2:8][S:9][CH2:10][CH2:11][NH:12][C:13]([NH:17][CH3:18])=[N:14][C:15]#[N:16])[N:3]=1.[F:19][C:20]([F:26])([F:25])[CH2:21][N:22]=[C:23]=S.[N:27]1C=CC=CC=1>>[F:19][C:20]([F:26])([F:25])[CH2:21][N:22]=[C:23]([NH2:27])[NH:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH2:8][S:9][CH2:10][CH2:11][NH:12][C:13]([NH:14][C:15]#[N:16])=[N:17][CH3:18])[N:3]=1Participants
Procedure
A mixture of 4-amino-2-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]pyrimidine (0.5 g.), 2,2,2-trifluoroethylisothiocyanate (0.55 g.) and pyridine (10 ml.) was heated at 70° for 18 hours and then evaporated to dryness. The residue was dissolved in ethyl acetate and the solution washed with 2N aqueous acetic acid, dried and evaporated to dryness. The residue was dissolved in ethanolic ammonia (15 ml.), treated with yellow mercuric oxide (0.4 g.) and the mixture stirred at room temperature for 4 hours. The mixture was filtered and the filtrate evaporated to dryness. The residue was purified by preparative thin layer chromatography using ethyl acetate/methanol/ammonia 6:1:0.5 v/v/v as developing solvent to give 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[2-(3-cyano-2-methylguanidino)ethylthiomethyl]pyrimidine (0.2 g.) characterised as the hydrogen maleate, m.p. 111°-114° (decomp.) after recrystallisation from acetonitrile.
Workup
- temperaturewas heated at 70° for 18 hours
- customevaporated to dryness
- dissolutionThe residue was dissolved in ethyl acetate
- washthe solution washed with 2N aqueous acetic acid
- customdried
- customevaporated to dryness
- dissolutionThe residue was dissolved in ethanolic ammonia (15 ml.)
- additiontreated with yellow mercuric oxide (0.4 g.)
- filtrationThe mixture was filtered
- customthe filtrate evaporated to dryness
- customThe residue was purified by preparative thin layer chromatography
Sources & evidence
- ORD record
- ord-fde28169ae7b4666a018551f7f1d8772
- Source dataset
- uspto-grants-1988_08
- Patent number
- US04762932
Linked notes
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