Nitrogen → 5-iodo-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole

HRID 2209133Notes

Reaction equation

HRID 2209133 reaction equation
N#N.[O:3]1[CH2:8][CH2:7][CH:6](O)[CH2:5][CH2:4]1.[I:10][C:11]1[NH:15][N:14]=[CH:13][CH:12]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C>C1COCC1>[I:10][C:11]1[N:15]([CH:6]2[CH2:7][CH2:8][O:3][CH2:4][CH2:5]2)[N:14]=[CH:13][CH:12]=1

Participants

7

Procedure

To a round-bottomed flask equipped with a stirring bar and a N2 tee, tetrahydro-2H-pyran-4-ol (1.05 g, 10.31 mmol), 5-iodo-1H-pyrazole (2.00 g, 10.31 mmol), triphenylphosphine (3.33 g, 12.68 mmol), (g, mmol) and THF (22.9 mL) were added. Followed by the addition of DIAD (2.71 g, 13.4 mmol), the resulting mixture was stirred at room temperature for 3 hrs. The mixture was removed most solvents in vauo, and ethyl acetate (200 mL) was added. The resulting solution were washed with H2O (50 mL×1), brine (50 mL×1), and dried over Na2SO4. The organic phase was filtered and removed solvent in vacuo, and passed a silica gel column (ethyl acetate: hexanes=0:100 to 100:0), off-white solids were obtained as the desired product. 920 mg (yield 32.1%). 1H NMR (300 MHz, DMSO-d6) δ 7.63-7.47 (m, 1H), 6.62-6.38 (m, 1H), 4.48 (tt, J=11.4, 4.3 Hz, 1H), 3.96 (ddt, J=11.8, 4.7, 1.2 Hz, 2H), 3.49 (td, J=12.0, 2.1 Hz, 2H), 2.00 (dddd, J=13.1, 12.0, 11.2, 4.6 Hz, 2H), 1.90-1.71 (m, 2H) ppm; MS (ESI+) m/z 279.30 (M+H).

Workup

  1. customTo a round-bottomed flask equipped with a stirring bar
  2. customThe mixture was removed most solvents in vauo, and ethyl acetate (200 mL)
  3. additionwas added
  4. washThe resulting solution were washed with H2O (50 mL×1), brine (50 mL×1)
  5. dry with materialdried over Na2SO4
  6. filtrationThe organic phase was filtered
  7. customremoved solvent in vacuo

Sources & evidence

ORD record
ord-db337f8b8de449a1bd9c8fea27def022
Source dataset
uspto-grants-2016_06
Patent number
US09376441B2

Reaction notes

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