Tris(1,1-dimethylethyl)phosphine → 5-[4-amino-3-(trifluoromethoxy)phenyl]-1-methyl-1H-pyrrole-2-carbonitrile

HRID 1591834Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1591834
Br[C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([O:9][C:10]([F:13])([F:12])[F:11])[CH:3]=1.[C:14]([C:16]1[N:20]([CH3:21])[C:19](B(O)O)=[CH:18][CH:17]=1)#[N:15].[F-].[K+].C(P(C(C)(C)C)C(C)(C)C)(C)(C)C>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[NH2:6][C:5]1[CH:7]=[CH:8][C:2]([C:19]2[N:20]([CH3:21])[C:16]([C:14]#[N:15])=[CH:17][CH:18]=2)=[CH:3][C:4]=1[O:9][C:10]([F:13])([F:12])[F:11]

Komponenten

6

Versuchsvorschrift

4-Bromo-2-(trifluoromethoxy)aniline (1.3 g, 5.0 mmol), 5-cyano-1-methyl-1H-pyrrol-2-yl boronic acid (0.9 g, 6.0 mmol), potassium fluoride (0.96 g, 16.5 mmol), and tris(dibenzylideneacetone)dipalladium (0.12 g, 0.12 mmol) were placed in an oven dried flask under nitrogen and THF (12.5 mL) was added. Tri-t-butylphosphine (10 wt % in hexane) (0.356 mL, 0.24 mol) was added and the reaction was stirred for 16 hours. The reaction mixture was filtered through silica, rinsed with ethyl acetate, and concentrated. The crude product was pre-adsorbed onto the Celite™ reagent and purified via Isco chromatography (the Redisep® column, silica, gradient 5-30% ethyl acetate in hexane) to afford 1.0 g (71%) of 5-[4-amino-3-(trifluoromethoxy)phenyl]-1-methyl-1H-pyrrole-2-carbonitrile.

Aufarbeitung

  1. customdried flask under nitrogen
  2. additionTHF (12.5 mL) was added
  3. filtrationThe reaction mixture was filtered through silica
  4. washrinsed with ethyl acetate
  5. concentrationconcentrated
  6. custompurified via Isco chromatography (the Redisep® column, silica, gradient 5-30% ethyl acetate in hexane)

Quellen und Nachweise

ORD-Eintrag
ord-ea220ee8fa194283bd03f23705775c9e
Quelldatensatz
uspto-grants-2007_11
Patentnummer
US07291643B2

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