3-(4-Hydroxyphenyl)propionic acid → N-(2,4-difluorobenzyl)-3-(4-hydroxyphenyl)-N-propylpropanamide

HRID 899893Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 899893
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][C:10]([OH:12])=O)=[CH:4][CH:3]=1.[F:13][C:14]1[CH:24]=[C:23]([F:25])[CH:22]=[CH:21][C:15]=1[CH2:16][NH:17][CH2:18][CH2:19][CH3:20].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.CCN(C(C)C)C(C)C.C(=O)([O-])O.[Na+]>CN(C=O)C>[F:13][C:14]1[CH:24]=[C:23]([F:25])[CH:22]=[CH:21][C:15]=1[CH2:16][N:17]([CH2:18][CH2:19][CH3:20])[C:10](=[O:12])[CH2:9][CH2:8][C:5]1[CH:4]=[CH:3][C:2]([OH:1])=[CH:7][CH:6]=1

Komponenten

7

Versuchsvorschrift

3-(4-Hydroxyphenyl)propionic acid (245 mg, 1.474 mmol) in DMF (5 ml) was cooled in an ice-bath. N-(2,4-Difluorobenzyl)-N-propylamine (300.4 mg, 1.622 mmol) was added and then TBTU (521 mg, 1.622 mmol) followed by DIPEA (400 mg, 3.096 mmol). The mixture was stirred at room temperature overnight. Sodium hydrogencarbonate aqueous solution (sat.) was added. The mixture was extracted with ethyl acetate (×2). The extracts were combined and dried (magnesium sulphate) and evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 5 g/25 ml) using DCM/heptane (50:50), DCM and then MeOH/DCM (1:99, then 2:98) as eluant gave 336 mg the desired product, yield 68%.

Aufarbeitung

  1. extractionThe mixture was extracted with ethyl acetate (×2)
  2. dry with materialdried (magnesium sulphate)
  3. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-3ce818fdfd1441a98695c0d1f53b0c77
Quelldatensatz
uspto-grants-2008_04
Patentnummer
US07355069B2

Notizen zur Reaktion

Wird geladen…