Hydrazine hydrate (1:1) → HCID 178469319, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[C:13]([C:14]([O:16][CH3:17])=[O:15])=[C:12]([CH3:18])[NH:11][C:10]([CH2:19][O:20][CH2:21][CH2:22][NH:23][C:24](=[N:27][C:28]#[N:29])SC)=[C:9]1[C:30]([O:32][CH2:33][CH3:34])=[O:31].O.[NH2:36][NH2:37]>C(O)C>[NH2:29][C:28]1[N:27]=[C:24]([NH:23][CH2:22][CH2:21][O:20][CH2:19][C:10]2[NH:11][C:12]([CH3:18])=[C:13]([C:14]([O:16][CH3:17])=[O:15])[CH:8]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[Cl:1])[C:9]=2[C:30]([O:32][CH2:33][CH3:34])=[O:31])[NH:37][N:36]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-{2-[(4-{2-Chlorophenyl}-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyrid-2-yl)methoxy]ethyl}-N'-cyano-S-methyl-isothiourea (0.4 g) and hydrazine hydrate (0.15 ml) were dissolved in ethanol (20 ml) and heated under reflux for 3 hours. The solvent was then evaporated and toluene (10 ml) was added to the residue, and again the solution was evaporated to dryness. The residue was chromatographed on Merck "Kieselgel 60H" (Trade Mark), eluting with 2% methanol is methylene chloride, to give a beige solid. The solid was recrystallised from ethyl acetate plus a trace of ether to give the title compound, yield 0.1 g, m.p. 137°-138°.
Workup
- temperatureheated
- temperatureunder reflux for 3 hours
- customThe solvent was then evaporated
- additiontoluene (10 ml) was added to the residue
- customagain the solution was evaporated to dryness
- customThe residue was chromatographed on Merck "Kieselgel 60H" (Trade Mark)
- washeluting with 2% methanol
- customto give a beige solid
- customThe solid was recrystallised from ethyl acetate
Sources & evidence
- ORD record
- ord-e36a3406cab44aa9b995e0e776260e50
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04670449
Reaction notes
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