Triphenylphosphine → Ethyl 6-{4-chloro-3-[(1-methylpyrrolidin-3-yl)oxy]phenyl}-5-(2,6-dimethoxyphenyl)pyridine-2-carboxylate

HRID 1639896Notes

Reaction equation

HRID 1639896 reaction equation
[CH3:1][N:2]1[CH2:6][CH2:5][CH:4]([OH:7])[CH2:3]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Cl:27][C:28]1[CH:33]=[CH:32][C:31]([C:34]2[N:39]=[C:38]([C:40]([O:42][CH2:43][CH3:44])=[O:41])[CH:37]=[CH:36][C:35]=2[C:45]2[C:50]([O:51][CH3:52])=[CH:49][CH:48]=[CH:47][C:46]=2[O:53][CH3:54])=[CH:30][C:29]=1O.CC(OC(/N=N/C(OC(C)C)=O)=O)C>C1COCC1.CCOC(C)=O>[Cl:27][C:28]1[CH:29]=[CH:30][C:31]([C:34]2[N:39]=[C:38]([C:40]([O:42][CH2:43][CH3:44])=[O:41])[CH:37]=[CH:36][C:35]=2[C:45]2[C:50]([O:51][CH3:52])=[CH:49][CH:48]=[CH:47][C:46]=2[O:53][CH3:54])=[CH:32][C:33]=1[O:7][CH:4]1[CH2:5][CH2:6][N:2]([CH3:1])[CH2:3]1

Participants

7

Reactant 4

HCID 11776TriphenylphosphineHCID 930741-Methyl-3-pyrrolidinolHCID 5363146Diisopropyl azodicarboxylateHCID 66720714Ethyl 6-(4-chloro-3-hydroxyphenyl)-5-(2,6-dimethoxyphenyl)pyridine-2-carboxylate

Product 1

HCID 66720745Ethyl 6-{4-chloro-3-[(1-methylpyrrolidin-3-yl)oxy]phenyl}-5-(2,6-dimethoxyphenyl)pyridine-2-carboxylateYield 70%

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolvent2×HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
0 °C

Procedure

Add 88 mg (0.87 mmol) of 1-methyl-3-hydroxypyrrolidine, 246 mg (1.09 mmol) of triphenylphosphine and 0.01 mL (0.07 mmol) of TEA to a solution of 300 mg (0.72 mmol) of ethyl 6-(4-chloro-3-hydroxyphenyl)-5-(2,6-dimethoxyphenyl)pyridine-2-carboxylate in 2.5 mL of anhydrous THF cooled to 0° C. and placed under argon. After dissolution, add dropwise, at 0° C., a solution of 0.24 mL (1.09 mmol) of DIAD in 2.5 mL of anhydrous THF. Bring the reaction mixture to RT, stir for 18 h, then take up in 50 mL of EtOAc. Wash the organic phase successively with 20 mL of a saturated aqueous solution of sodium bicarbonate (NaHCO3) then 20 mL of water. After drying over Na2SO4 and concentration under reduced pressure, purify the residue obtained by silica gel column chromatography, eluting with a DCM/methanol gradient from 0 to 20% of methanol. After concentration under reduced pressure, we obtain 250 mg of ethyl 6-{4-chloro-3-[(1-methylpyrrolidin-3-yl)oxy]phenyl}-5-(2,6-dimethoxyphenyl)pyridine-2-carboxylate in the form of oil.

Workup

  1. dissolutionAfter dissolution
  2. additionadd dropwise, at 0° C.
  3. customto RT
  4. washWash the organic phase successively with 20 mL of a saturated aqueous solution of sodium bicarbonate (NaHCO3)
  5. dry with materialAfter drying over Na2SO4 and concentration under reduced pressure
  6. custompurify the residue
  7. customobtained by silica gel column chromatography
  8. washeluting with a DCM/methanol gradient from 0 to 20% of methanol
  9. concentrationAfter concentration under reduced pressure, we

Sources & evidence

ORD record
ord-d7c58acd6547488b9883e3c5ade1abfc
Source dataset
uspto-grants-2012_02
Patent number
US08110579B2

Reaction notes

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