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Hexane → [2-(4-Chloro-phenyl)-2H-indazol-3-yl]-cyclohexyl-methanol

HRID 1678625
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1678625
C([Li])CCC.CCCCCC.CCN(C(C)C)C(C)C.[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([N:28]2[CH:36]=[C:35]3[C:30]([CH:31]=[CH:32][CH:33]=[CH:34]3)=[N:29]2)=[CH:24][CH:23]=1.[CH:37]1([CH:43]=[O:44])[CH2:42][CH2:41][CH2:40][CH2:39][CH2:38]1>C1COCC1>[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([N:28]2[C:36]([CH:43]([CH:37]3[CH2:42][CH2:41][CH2:40][CH2:39][CH2:38]3)[OH:44])=[C:35]3[C:30]([CH:31]=[CH:32][CH:33]=[CH:34]3)=[N:29]2)=[CH:24][CH:23]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 8058HexaneHCID 16275CyclohexanecarboxaldehydeHCID 81531DiisopropylethylamineHCID 156367542-(4-Chlorophenyl)-2H-indazoleHCID 178418339Butyllithium

Produkt 1

HCID 67130979[2-(4-Chloro-phenyl)-2H-indazol-3-yl]-cyclohexyl-methanolAusbeute 43 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

A 1.6 M solution of n-butyllithium in hexane (5.7 ml, 9.1 mmol) was added within 10 min to a −78° C. cold solution of N,N′-diisopropylethylamine (1.55 ml, 9.1 mmol) in THF (25.5 ml). The solution was stirred for 10 min at 5° C. and cooled again to −78° C. A solution of 2-(4-chloro-phenyl)-2H-indazole (1.7 g, 7.4 mmol; Liu, Rui; Zhu, Yong-ming; Qin, Lie-na; Ji, Shun-jun; Katayama, Haji. Heterocycles (2007), 71(8), 1755-1763.) in THF (8.5 ml) was added, the suspension was stirred for 15 min at 0° C., cooled to −78° C. and cyclohexane-carbaldehyde (1.1 ml, 9.1 mmol; CAS Reg. No. 2043-61-0) was added. The reaction mixture was stirred at ambient temperature for 14 h. Under ice cooling saturated aqueous ammonium chloride solution was added and the mixture was extracted two times with iPrOAc. The combined extracts were washed with ice water/brine 1/1 and dried over Na2SO4. After filtration the solvent was removed under reduced pressure and the residue was purified by column chromatography (silica gel, iPrOAc/heptane) to give the title compound (1.1 g, 3.2 mmol; 43%) as yellow foam. MS: m/e=341.2 [M+H+].

Aufarbeitung

  1. temperaturecooled again to −78° C
  2. stirringthe suspension was stirred for 15 min at 0° C.
  3. temperaturecooled to −78° C.
  4. addition2043-61-0) was added
  5. stirringThe reaction mixture was stirred at ambient temperature for 14 h
  6. additionUnder ice cooling saturated aqueous ammonium chloride solution was added
  7. extractionthe mixture was extracted two times with iPrOAc
  8. washThe combined extracts were washed with ice water/brine 1/1
  9. dry with materialdried over Na2SO4
  10. filtrationAfter filtration the solvent
  11. customwas removed under reduced pressure
  12. customthe residue was purified by column chromatography (silica gel, iPrOAc/heptane)

Quellen und Nachweise

ORD-Eintrag
ord-c33e5113487747a99d35aa60b656c5a0
Quelldatensatz
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08008505B2

Notizen zur Reaktion

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