Sodium Hydroxide → HCID 178424071, compound

HRID 1353754Notes

Reaction equation

HRID 1353754 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2(C(C3CCCCO3)=O)[C:16]3[C:11](=[CH:12][CH:13]=[C:14]([C:17]4[N:21]=[CH:20][N:19](C5C=CC(C)=C(C)C=5C)[N:18]=4)[CH:15]=3)[NH:10][NH:9]2)=[CH:4][CH:3]=1.[OH-].[Na+]>Cl.O1CCOCC1>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[C:14]([C:17]4[N:21]=[CH:20][NH:19][N:18]=4)[CH:15]=3)[NH:10][N:9]=2)=[CH:4][CH:3]=1

Participants

5

Reactant 2

HCID 14798Sodium HydroxideHCID 69425736HCID 69425736, compound

Product 1

HCID 178424071HCID 178424071, compoundYield 40%

Reagents, catalysts & solvents 2

HCID 313Hydrochloric AcidSolvent2×HCID 312751,4-DioxaneSolvent

Procedure

2-{3-(4-Methylphenyl)-5-[1-(trimethylphenyl)(1,2,4-triazol-3-yl)]-1H-indazoyl}perhydro-2H-pyran (0.130 g, 0.216 mmol) was dissolved in 4 mL of 4.0 N HCl in dioxane and 2 mL of 6.0 N aqueous HCl were added. After 2 hours at room temperature, the reaction mixture was neutralized using aqueous sodium hydroxide (6.0 N) and the product was extracted with ethyl acetate. The extracts were dried under vacuum and dissolved in 5 mL of 6.0 N aqueous sodium hydroxide, side products extracted twice with diethyl ether. The aqueous phase was neutralized with 6.0 N HCl and the product was extracted with ethyl acetate. The crude was purified by preparative HPLC (15–80% acetonitrile in water) (0.024 g, 40% yield): 1H NMR (DMSO-d6) δ 13.4 (br s, 1H), 8.7 (s, 1H), 8.4 (br s, 1H), 8.1 (dd, 1H), 7.9 (d, 2H), 7.7 (d, 1H), 7.4 (d, 2H), 7.0 (d, 1H), 2.4 (s, 3H); ES-MS (m/z) 276 [M+1]+.

Workup

  1. extractionthe product was extracted with ethyl acetate
  2. customThe extracts were dried under vacuum
  3. dissolutiondissolved in 5 mL of 6.0 N aqueous sodium hydroxide
  4. extractionside products extracted twice with diethyl ether
  5. extractionthe product was extracted with ethyl acetate
  6. customThe crude was purified by preparative HPLC (15–80% acetonitrile in water) (0.024 g, 40% yield)

Sources & evidence

ORD record
ord-d32c60ddd5be46e5bed88ed1d7a7fd8f
Source dataset
uspto-grants-2007_05
Patent number
US07220771B2

Reaction notes

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