Pyridine, hydrofluoride (1:1) → 2-(4-Hydroxyphenethyl)-6-phenylpyridazin-3(2h)-one

HRID 1878761Notes

Reaction equation

HRID 1878761 reaction equation
[Si]([O:8][C:9]1[CH:29]=[CH:28][C:12]([CH2:13][CH2:14][N:15]2[C:20](=[O:21])[CH:19]=[CH:18][C:17]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[N:16]2)=[CH:11][CH:10]=1)(C(C)(C)C)(C)C.C1C=CN=CC=1.F>C(#N)C>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:13][CH2:14][N:15]2[C:20](=[O:21])[CH:19]=[CH:18][C:17]([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)=[N:16]2)=[CH:28][CH:29]=1

Participants

4

Reactant 2

HCID 64774Pyridine, hydrofluoride (1:1)HCID 598430232-(4-(tert-Butyldimethylsilyloxy)phenethyl)-6-phenylpyridazin-3(2H)-one

Product 1

HCID 598430212-(4-Hydroxyphenethyl)-6-phenylpyridazin-3(2h)-one

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

To a stirring solution of 2-(4-(tert-butyldimethylsilyloxy)phenethyl)-6-phenylpyridazin-3(2H)-one (180 mg, 443 μmol) in ACN (3 mL) was added 70% HF-pyridine (0.25 mL) at 23° and stirred for 18 h. Solvents removed under reduced pressure and residue partioned between 9:1 CHCl3/iPrOH (30 mL) and 5% NaHCO3 (15 mL). The aqueous was further extracted with 9:1 CH3Cl/iPrOH (3×20 mL). Combined organics dried over MgSO4 then concentrated to a solid under reduced pressure from toluene. The residue was purified on 40 grams of silica eluting with 0-% EtOAc/CH2Cl2. The isolated solid was recrystallized from ACN (1 mL). MS (ESI pos. ion) m/z (MH+): 293. Calc'd exact mass for C18H16N2O2: 292. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.97 (t, J=7.28 Hz, 2 H) 3.17 (s, 1 H) 4.31 (t, J=7.53 Hz, 2 H) 6.66 (d, J=8.53 Hz, 2 H) 7.02 (t, J=8.28 Hz, 3 H) 7.39-7.54 (m, 3 H) 7.82 (d, J=8.03 Hz, 2 H) 8.01 (d, J=9.54 Hz, 1 H) 9.20 (s, 1 H).

Workup

  1. customSolvents removed under reduced pressure and residue partioned between 9:1 CHCl3/iPrOH (30 mL) and 5% NaHCO3 (15 mL)
  2. extractionThe aqueous was further extracted with 9:1 CH3Cl/iPrOH (3×20 mL)
  3. dry with materialCombined organics dried over MgSO4
  4. concentrationthen concentrated to a solid under reduced pressure from toluene
  5. customThe residue was purified on 40 grams of silica eluting with 0-% EtOAc/CH2Cl2
  6. customThe isolated solid was recrystallized from ACN (1 mL)

Sources & evidence

ORD record
ord-694ee6fa0a9548c8991170d4cf3bbc60
Source dataset
uspto-grants-2012_11
Patent number
US08314087B2

Reaction notes

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