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Methanol → (R)-6-(3-methyl-1-(4'-(trifluoromethyl)biphenyl-4-yl)butylamino)nicotinic acid

HRID 2406920
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2406920
C[O:2][C:3](=[O:32])[C:4]1[CH:9]=[CH:8][C:7]([NH:10][C@@H:11]([C:16]2[CH:21]=[CH:20][C:19]([C:22]3[CH:27]=[CH:26][C:25]([C:28]([F:31])([F:30])[F:29])=[CH:24][CH:23]=3)=[CH:18][CH:17]=2)[CH2:12][CH:13]([CH3:15])[CH3:14])=[N:6][CH:5]=1.CO.[OH-].[Na+]>O1CCCC1>[CH3:14][CH:13]([CH3:15])[CH2:12][C@@H:11]([NH:10][C:7]1[CH:8]=[CH:9][C:4]([C:3]([OH:32])=[O:2])=[CH:5][N:6]=1)[C:16]1[CH:17]=[CH:18][C:19]([C:22]2[CH:23]=[CH:24][C:25]([C:28]([F:31])([F:30])[F:29])=[CH:26][CH:27]=2)=[CH:20][CH:21]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 67980699(R)-methyl-6-(3-methyl-1-(4'-(trifluoromethyl)biphenyl-4-yl)butylamino)nicotinate

Produkt 1

HCID 67981033(R)-6-(3-methyl-1-(4'-(trifluoromethyl)biphenyl-4-yl)butylamino)nicotinic acidAusbeute 90,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A round bottom flask was charged with (R)-methyl-6-(3-methyl-1-(4′-(trifluoromethyl)biphenyl-4-yl)butylamino)nicotinate (41.5 g, 93.8 mmol), methanol (200 mL) and tetrahydrofuran (200 mL). 1.0N NaOH (188 mL) was then added and the resulting solution was stirred at 50° C. for 3 hours. The reaction was cooled to room temperature and the organic solvents removed under reduced pressure. Water (300 mL) was added and the mixture was acidified with 10% citric acid to pH=3. A white precipitate formed and the heterogeneous mixture was stirred for 30 minutes at 0° C. The mixture was then filtered and the solid was dried under reduced pressure to afford (R)-6-(3-methyl-1-(4′-(trifluoromethyl)biphenyl-4-yl)butylamino)nicotinic acid (36.2 g, 90.0%). 1H NMR (400 MHz, CDCl3, δ): 0.98 (d, J=6.46 Hz, 3 H) 1.03 (d, J=6.46 Hz, 3 H) 1.66-1.78 (m, 1 H) 1.78-1.89 (m, 1 H) 1.96-2.05 (m, 1 H) 4.49-4.63 (m, 1 H) 6.44 (d, J=9.00 Hz, 1 H) 7.44-7.50 (m, 2 H) 7.53-7.58 (m, 2 H) 7.63-7.70 (m, 4 H) 8.17 (d, J=9.19 Hz, 1 H) 8.69-8.74 (m, 1 H) 9.44 (br. s., 1 H). MS (M+1): 429.4.

Aufarbeitung

  1. temperatureThe reaction was cooled to room temperature
  2. customthe organic solvents removed under reduced pressure
  3. additionWater (300 mL) was added
  4. customA white precipitate formed
  5. stirringthe heterogeneous mixture was stirred for 30 minutes at 0° C
  6. filtrationThe mixture was then filtered
  7. customthe solid was dried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b45c4515e7054b2b89ce9cba979c251f
Quelldatensatz
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08809342B2

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