Acetic Acid → 2-[3,5-Dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-3,5-dioxo-2,3,4,5-tetrahydro-[1,2,4]triazine-6-carbonitrile

HRID 1157256Notes

Reaction equation

HRID 1157256 reaction equation
C([O:3][C:4](=O)[NH:5][C:6](=[O:32])[C:7]([C:30]#[N:31])=[N:8][NH:9][C:10]1[CH:15]=[C:14]([Cl:16])[C:13]([O:17][C:18]2[CH:23]=[C:22]([CH:24]([CH3:26])[CH3:25])[C:21](=[O:27])[N:20]([CH3:28])[N:19]=2)=[C:12]([Cl:29])[CH:11]=1)C.C([O-])(=O)C.[K+].C(O)(=O)C.O>CN(C)C(=O)C.C(#N)C>[Cl:29][C:12]1[CH:11]=[C:10]([N:9]2[C:4](=[O:3])[NH:5][C:6](=[O:32])[C:7]([C:30]#[N:31])=[N:8]2)[CH:15]=[C:14]([Cl:16])[C:13]=1[O:17][C:18]1[CH:23]=[C:22]([CH:24]([CH3:26])[CH3:25])[C:21](=[O:27])[N:20]([CH3:28])[N:19]=1

Participants

7

Reactant 4

HCID 176Acetic AcidHCID 962WaterHCID 517044Potassium AcetateHCID 72574122(2-Cyano-2-{[3,5-dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-hydrazono}-acetyl)-carbamic acid ethyl ester

Product 1

HCID 120011102-[3,5-Dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-3,5-dioxo-2,3,4,5-tetrahydro-[1,2,4]triazine-6-carbonitrileYield 85.8%

Reagents, catalysts & solvents 2

HCID 6342AcetonitrileSolventHCID 31374DimethylacetamideSolvent

Procedure

A solution of (2-cyano-2-{[3,5-dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-hydrazono}-acetyl)-carbamic acid ethyl ester (68) (6.5 g, 13.12 mmol) and potassium acetate (1.42 g, 14.43 mmol) in N,N-dimethylacetamide was heated to 120° C. for 2 h. At this time, the reaction was cooled to room temperature and was treated with glacial acetic acid (1.5 mL) and water (65 mL). The mixture was stirred at room temperature for 15 min. The solids which resulted were collected by filtration, washed with water (65 mL) and dried under vacuum to give an orange solid. The solid was suspended in acetonitrile (36 mL), heated to reflux for 3 h and then cooled to room temperature. The resulting solids were then collected by filtration, washed with acetonitrile (12 mL) and methyl tert-butyl ether (24 mL) and dried under vacuum to afford 2-[3,5-dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-3,5-dioxo-2,3,4,5-tetrahydro[1,2,4]triazine-6-carbonitrile (69) (5.06 g, 85.8%) as an orange solid; ES(+)-HRMS m/e calcd for C18H14Cl2N6O4 (M+H)+ 449.0527, found 449.0527. Exact Mass=448.0454; Molecular Weight=449.26.

Workup

  1. customThe solids which resulted
  2. filtrationwere collected by filtration
  3. washwashed with water (65 mL)
  4. customdried under vacuum
  5. customto give an orange solid
  6. temperatureheated
  7. temperatureto reflux for 3 h
  8. temperaturecooled to room temperature
  9. filtrationThe resulting solids were then collected by filtration
  10. washwashed with acetonitrile (12 mL) and methyl tert-butyl ether (24 mL)
  11. customdried under vacuum

Sources & evidence

ORD record
ord-b05f74cb98d5492189aebba783372ce8
Source dataset
uspto-grants-2010_10
Patent number
US07807674B2

Reaction notes

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