Water → Methyl [4-cyano-1-(trifluoroacetyl)-2,3-dihydro-1h-1-benzazepin-2-yl]acetate

HRID 1761028Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1761028
[F:1][C:2]([F:30])([F:29])[C:3]([N:5]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH:9]=[C:8](OS(C(F)(F)F)(=O)=O)[CH2:7][CH:6]1[CH2:24][C:25]([O:27][CH3:28])=[O:26])=[O:4].[Li][C:32]#[N:33].C1OCCOCCOCCOC1.O>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:32]([C:8]1[CH2:7][CH:6]([CH2:24][C:25]([O:27][CH3:28])=[O:26])[N:5]([C:3](=[O:4])[C:2]([F:29])([F:1])[F:30])[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH:9]=1)#[N:33]

Komponenten

7

Versuchsvorschrift

A solution of the compound obtained in Step e (1.35 g; 293 mmol) in 16 ml of anhydrous toluene is added to a mixture of LiCN (0.5 M in DMF) (11.72 ml; 5.86 mmol), (Ph3P)4Pd (237 mg; 0.205 mmol) and 12-crown-4 (36 mg; 0.205 mmol) under an argon. atmosphere. The reaction mixture is stirred at ambient temperature for 6 hours. Water (10 ml) is added to the reaction mixture, and the organic phase is extracted with diethyl ether. After drying and concentration, the residue obtained is purified on silica gel (eluant:heptane/EtOAc) to yield the title product.

Aufarbeitung

  1. extractionthe organic phase is extracted with diethyl ether
  2. customAfter drying
  3. concentrationconcentration
  4. customthe residue obtained
  5. customis purified on silica gel (eluant:heptane/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-509b45decb944185882a990907552a84
Quelldatensatz
uspto-grants-2005_01
Patentnummer
US06846833B2

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