Tetrahydrofuran → HCID 9863870, compound

HRID 1936737Notes

Reaction equation

HRID 1936737 reaction equation
C([O:3][C:4]([CH:6]1[CH2:11][CH2:10][C:9]([C:12]2[CH:20]=[C:19]3[C:15]([C:16]([CH2:28][CH3:29])=[N:17][N:18]3[C:21]3[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=3)=[CH:14][CH:13]=2)=[CH:8][CH2:7]1)=[O:5])C.O1CCCC1.[OH-].[Na+]>CO>[CH2:28]([C:16]1[C:15]2[C:19](=[CH:20][C:12]([C:9]3[CH2:10][CH2:11][CH:6]([C:4]([OH:5])=[O:3])[CH2:7][CH:8]=3)=[CH:13][CH:14]=2)[N:18]([C:21]2[CH:22]=[CH:23][C:24]([F:27])=[CH:25][CH:26]=2)[N:17]=1)[CH3:29]

Participants

5

Procedure

To a stirred solution of 1.13 g (2.87 mmol) of 4-(3-ethyl-1-(4-fluorophenyl)-1H-indazol-6-yl)-cyclohex-3-ene-carboxylic acid ethyl ester dissolved in 50 mL of methanol and 15 mL of tetrahydrofuran was added 8.62 mL (8.61 mmol) of 1N sodium hydroxide and reaction mixture heated to reflux for 3 hr. After 3 hr, the reaction mixture was concentrated on a rotary evaporator, diluted with 200 mL of H2O, acidified to pH 1 with 1N HCl and extracted 2×200 mL ethyl acetate. The organic extracts were combined, washed with water, brine and dried over Na2SO4. Filtration, concentration and drying gave crude product. Recrystallization from ethyl acetate/hexane gave 0.31 grams of white crystalline product mp=214-216° C.; MS, m/z 365 (M+H+, base).

Workup

  1. temperatureheated
  2. temperatureto reflux for 3 hr
  3. concentrationthe reaction mixture was concentrated on a rotary evaporator
  4. additiondiluted with 200 mL of H2O
  5. extractionextracted 2×200 mL ethyl acetate
  6. washwashed with water, brine
  7. dry with materialdried over Na2SO4
  8. filtrationFiltration, concentration
  9. customdrying
  10. customgave crude product
  11. customRecrystallization from ethyl acetate/hexane

Sources & evidence

ORD record
ord-4154e26bff084281836cfa1bd0dc0374
Source dataset
uspto-grants-2002_05
Patent number
US06391872B1

Reaction notes

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