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Phosphorus oxychloride → 4-Chloro-2,6-dihydro-2-methyl-6-(1-naphthalenylmethyl)-1H-pyrrolo[3,4-d]pyridazin-1-one

HRID 1835152
Notes
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Reaction equation

HRID 1835152 reaction equation
[CH3:1][N:2]1[C:7](=[O:8])[C:6]2=[CH:9][N:10]([CH2:12][C:13]3[C:22]4[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=4)[CH:16]=[CH:15][CH:14]=3)[CH:11]=[C:5]2[C:4](=O)[NH:3]1.P(Cl)(Cl)([Cl:26])=O>>[Cl:26][C:4]1[C:5]2[C:6](=[CH:9][N:10]([CH2:12][C:13]3[C:22]4[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=4)[CH:16]=[CH:15][CH:14]=3)[CH:11]=2)[C:7](=[O:8])[N:2]([CH3:1])[N:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 235032482,3-Dihydro-2-methyl-6-(1-naphthalenylmethyl)-1H-pyrrolo[3,4-d]pyridazin-1,4(6H)-dione

Product 1

HCID 235032554-Chloro-2,6-dihydro-2-methyl-6-(1-naphthalenylmethyl)-1H-pyrrolo[3,4-d]pyridazin-1-one

Procedure

A suspension of 2,3-dihydro-2-methyl-6-(1-naphthalenylmethyl)-1H-pyrrolo[3,4-d]pyridazine-1,4(6H)-dione (0.10 g) in phosphorus oxychloride (1 ml) was heated at reflux for 30 minutes and then allowed to cool. The solvent was evaporated, water (25 ml) was added and the mixture was extracted with ethyl acetate (2×25 ml). The organic extracts were dried, filtered and evaporated to give the sub-title compound (0.095 g).

Workup

  1. temperature
was heated
  • temperatureat reflux for 30 minutes
  • temperatureto cool
  • customThe solvent was evaporated
  • additionwater (25 ml) was added
  • extractionthe mixture was extracted with ethyl acetate (2×25 ml)
  • customThe organic extracts were dried
  • filtrationfiltered
  • customevaporated
  • Sources & evidence

    ORD record
    ord-04184055b5ba49aabe789d109fd45c87
    Source dataset
    uspto-grants-2004_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06770646B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes