Methanol → HCID 58960088, compound

HRID 916152Notes

Reaction equation

HRID 916152 reaction equation
[C:1]([CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][C:10]1=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.[CH3:16][O:17][C:18](=[O:29])[C@H:19]([CH2:21][C:22]1[CH:27]=[CH:26][C:25]([OH:28])=[CH:24][CH:23]=1)[NH2:20].O.CO>C1(OC)C=CC=CC=1.[Pd]>[CH3:16][O:17][C:18](=[O:29])[CH:19]([NH:20][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[C:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1)[CH2:21][C:22]1[CH:27]=[CH:26][C:25]([OH:28])=[CH:24][CH:23]=1

Participants

7

Reactant 4

HCID 887MethanolHCID 962WaterHCID 70652Tyrosine Methyl EsterHCID 10512350HCID 10512350, compound

Product 1

HCID 58960088HCID 58960088, compoundYield 39%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 7519AnisoleSolvent

Conditions

Temperature
80 °C

Procedure

To a mixture of 2-nicotinoylcyclohexanone (914.0 g, 0.45 mol), L-tyrosine methyl ester (78.0 g, 0.40 mol) in anisole (1000 ml) is added 5% palladium on carbon (20 g), then the mixture is heated to reflux for 2 h while the resulting water is removed by a Dean-Stark apparatus. The mixture is cooled to 80° C., and the Pd/C is filtered and washed with anisole (3×60 ml). The mixture is cooled to 40° C., hexane (1000 ml) is added and the mixture kept at −20° C. for 48 h. The solid is filtered and washed with hexane (5×200 ml) to yield the crude 2-((2-nicotinoylphenyl)amino)-3-(4-hydroxyphenyl)-propionic acid methyl ester. The crude product is mixed with 250 ml of methanol and is refluxed for 30 min. After cooled to 0° C., the product is filtered, washed with methanol (2×50 ml), and dried under a vacuum to give the title compound (58.6 g, 39.0%).

Workup

  1. temperaturethe mixture is heated
  2. customis removed by a Dean-Stark apparatus
  3. filtrationthe Pd/C is filtered
  4. washwashed with anisole (3×60 ml)
  5. temperatureThe mixture is cooled to 40° C.
  6. additionhexane (1000 ml) is added
  7. filtrationThe solid is filtered
  8. washwashed with hexane (5×200 ml)
  9. customto yield the crude 2-((2-nicotinoylphenyl)amino)-3-(4-hydroxyphenyl)-propionic acid methyl ester
  10. temperatureis refluxed for 30 min
  11. temperatureAfter cooled to 0° C.
  12. filtrationthe product is filtered
  13. washwashed with methanol (2×50 ml)
  14. customdried under a vacuum

Sources & evidence

ORD record
ord-c66cee5ffc434851b3aa4d7d14888395
Source dataset
uspto-grants-2007_09
Patent number
US07268157B2

Reaction notes

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