Hydrochloric Acid → HCID 59678687, compound

HRID 1392865Notes

Reaction equation

HRID 1392865 reaction equation
[C:1]([N:5]1[C:10](=[O:11])[C:9]([CH2:12]Br)=[C:8]([Cl:14])[CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-:16].[Ca+2].O1CCOCC1.O.Cl>O1CCOCC1>[C:1]([N:5]1[C:10](=[O:11])[C:9]([CH2:12][OH:16])=[C:8]([Cl:14])[CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 10112Calcium CarbonateHCID 19081406HCID 19081406, compoundHCID 218864351,4-Dioxane--water (1/1)

Product 1

HCID 59678687HCID 59678687, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

2-tert-butyl-4-bromomethyl-5-chloro 3(2H)-pyridazinone (2 g, 7.19 mmol) and calcium carbonate (3.5 gm) are added to a 1:1 mixture of dioxane-water (40 ml). The mixture is refluxed for 6 hours after which 30 ml of 3N HCl solution is added to it. The solution is stirred for 10 minutes after which dioxane is removed under reduced pressure. The resulting solution is then extracted with dichloromethane and the dichloromethane layer is washed and dried. The crude obtained after concentration is purified by flash chromatography (ethyl acetate/hexanes: 1:2).

Workup

  1. additionis added to it
  2. customis removed under reduced pressure
  3. extractionThe resulting solution is then extracted with dichloromethane
  4. washthe dichloromethane layer is washed
  5. customdried
  6. customThe crude obtained
  7. concentrationafter concentration
  8. customis purified by flash chromatography (ethyl acetate/hexanes: 1:2)

Sources & evidence

ORD record
ord-c603409dea894767a10c6ca5b3864e28
Source dataset
uspto-grants-2008_03
Patent number
US07344702B2

Reaction notes

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