Hydrazine hydrate (1:1) → HCID 178469319, compound

HRID 652068Notes

Reaction equation

HRID 652068 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]=1

Participants

4

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

  1. temperatureheated
  2. temperatureunder reflux for 3 hours
  3. customThe solvent was then evaporated
  4. additiontoluene (10 ml) was added to the residue
  5. customagain the solution was evaporated to dryness
  6. customThe residue was chromatographed on Merck "Kieselgel 60H" (Trade Mark)
  7. washeluting with 2% methanol
  8. customto give a beige solid
  9. 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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