Hydrazine hydrate (1:1) → HCID 59651895, compound

HRID 1186869Notes

Reaction equation

HRID 1186869 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[C:20]([F:21])=[CH:19][C:18]([C:22](=O)[CH2:23][CH2:24][C:25](OCC)=[O:26])=[CH:17][C:16]=2[F:31])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].O.[NH2:33][NH2:34]>C(O)(C)C>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[C:20]([F:21])=[CH:19][C:18]([C:22]3[CH2:23][CH2:24][C:25](=[O:26])[NH:34][N:33]=3)=[CH:17][C:16]=2[F:31])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

4

Procedure

A mixture of 4-[4-(3-ethoxycarbonyl-propionyl)-2,6-difluoro-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester (3.21 g, 7.27 mmol) and hydrazine monohydrate (0.7 mL, 14.1 mmol) in isopropanol (20 mL) was stirred at reflux overnight. Isopropanol was concentrated at reduced pressure and partitioned between saturated aqueous sodium bicarbonate solution and methylene chloride. The aqueous layer was extracted twice with methylene chloride and the combined organics was washed with brine, dried (Na2SO4), filtered, and concentrated to provide a crude material. The crude material was purified by ISCO (80 g silica gel column) chromatography using 15 to 60% EtOAc in hexane to obtain 4-[2,6-difluoro-4-(6-oxo-1,4,5,6-tetrahydro-pyridazin-3-yl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester (0.42 g, 14%).

Workup

  1. temperatureat reflux overnight
  2. concentrationIsopropanol was concentrated at reduced pressure
  3. custompartitioned between saturated aqueous sodium bicarbonate solution and methylene chloride
  4. extractionThe aqueous layer was extracted twice with methylene chloride
  5. washthe combined organics was washed with brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto provide a crude material
  10. customThe crude material was purified by ISCO (80 g silica gel column) chromatography

Sources & evidence

ORD record
ord-2c3c4e732d46407caeb7b20fd90cae58
Source dataset
uspto-grants-2014_03
Patent number
US08673916B2

Reaction notes

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