1,2-Dichlorobenzene → 7-Allyl-1H-indazol-6-ol

HRID 2121856

Reaktionsgleichung

Reaktionsgleichung von HRID 2121856
C([O:4][C:5]1[CH:13]=[C:12]2[C:8]([CH:9]=[N:10][NH:11]2)=[CH:7][CH:6]=1)C=C.Cl[C:15]1[CH:20]=CC=C[C:16]=1Cl>>[CH2:20]([C:13]1[C:5]([OH:4])=[CH:6][CH:7]=[C:8]2[C:12]=1[NH:11][N:10]=[CH:9]2)[CH:15]=[CH2:16]

Komponenten

3

Edukt 2

HCID 72391,2-DichlorobenzeneHCID 224965696-Allyloxy-1H-indazole

Produkt 1

HCID 1358436477-Allyl-1H-indazol-6-olAusbeute 60 %

Versuchsvorschrift

A solution of the product from Step A (14.2 g, 82 mmol) in 1,2-dichlorobenzene (90 mL) was fluxed for 6 h and the reaction mixture was evaporated to a residue which was purified by chromatography (silica, EtOAc) to give a tan solid (8.59 g, 60%) that was used in the next step: LC/MS (+APCI) m/z 175 (M+H).

Aufarbeitung

  1. customthe reaction mixture was evaporated to a residue which
  2. customwas purified by chromatography (silica, EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-3fb586f8ecf842dd8ff01f5a4cd01c74
Quelldatensatz
uspto-grants-2004_02
Patentnummer
US06696476B2

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