Anisole → HCID 57422418, compound

HRID 2094947Notes

Reaction equation

HRID 2094947 reaction equation
[CH2:1]([N:8]1[CH2:13][N:12](CC2C=CC(OC)=CC=2OC)[CH2:11][N:10]([C:25]2[CH:26]=[N:27][N:28]([CH2:30][C:31]3[C:32]([CH3:37])=[N:33][O:34][C:35]=3[CH3:36])[CH:29]=2)[C:9]1=[O:38])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(OC)C=CC=CC=1.FC(F)(F)C(O)=O.ClCCl>ClCCl>[CH2:1]([N:8]1[CH2:13][NH:12][CH2:11][N:10]([C:25]2[CH:26]=[N:27][N:28]([CH2:30][C:31]3[C:32]([CH3:37])=[N:33][O:34][C:35]=3[CH3:36])[CH:29]=2)[C:9]1=[O:38])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

5

Reactant 3

HCID 7519AnisoleHCID 21863450Trifluoroacetic acid methylene chlorideHCID 57422419HCID 57422419, compound

Product 1

HCID 57422418HCID 57422418, compoundYield 62%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

1-benzyl-5-(2,4-dimethoxybenzyl)-3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1,3,5-triazinan-2-one (example 9-6a) (44 mg, 0.09 mmol), anisole (9 mg, 0.09 mmol), and 50% trifluoroacetic acid/dichloromethane solution (1 mL) in dichloromethane (1 mL) were stirred at room temperature for 2 hours. The reaction was concentrated, quenched with saturated sodium bicarbonate (50 mL), extracted with ethyl acetate (2×, 50 mL) and washed with brine (50 mL). The combined organic extracts were dried over magnesium sulfate, filtered and, concentrated. Purification by silica column chromotography (100% to 90% dichloromethane in methanol: 30 minute gradient) afforded 1-benzyl-3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1,3,5-triazinan-2-one (19 mg, 62%) as a white solid. LC/MS; [M+H] calculated for C19H22N6O2; expected 367.18; found 367.20. The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 5.84 μM.

Workup

  1. concentrationThe reaction was concentrated
  2. customquenched with saturated sodium bicarbonate (50 mL)
  3. extractionextracted with ethyl acetate (2×, 50 mL)
  4. washwashed with brine (50 mL)
  5. dry with materialThe combined organic extracts were dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification by silica column chromotography (100% to 90% dichloromethane in methanol: 30 minute gradient)

Sources & evidence

ORD record
ord-b8bca6a1906d4f0589b8566b1ebb0c43
Source dataset
uspto-grants-2013_05
Patent number
US08445692B2

Reaction notes

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