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Guaiacol → HCID 22054602, Verbindung

HRID 1006142
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1006142
CC(OC(/N=N/C(OC(C)C)=O)=O)C.Cl[C:16]1[C:25]2[C:20](=[CH:21][C:22]([CH2:26][OH:27])=[CH:23][CH:24]=2)[N:19]=[C:18]([CH3:28])[CH:17]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:48][O:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][C:51]=1O.[NH:57]1[CH2:61][CH2:60][CH2:59][CH2:58]1.[C:62]([OH:67])(=[O:66])[C:63]([OH:65])=[O:64]>ClCCl.C(O)C>[C:62]([OH:67])(=[O:66])[C:63]([OH:65])=[O:64].[CH3:48][O:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][C:51]=1[O:27][CH2:26][C:22]1[CH:21]=[C:20]2[C:25]([C:16]([N:57]3[CH2:61][CH2:60][CH2:59][CH2:58]3)=[CH:17][C:18]([CH3:28])=[N:19]2)=[CH:24][CH:23]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 6

HCID 460GuaiacolHCID 971Oxalic AcidHCID 11776TriphenylphosphineHCID 31268PyrrolidineHCID 5363146Diisopropyl azodicarboxylateHCID 11264243HCID 11264243, Verbindung

Produkt 1

HCID 22054602
HCID 22054602, Verbindung
Ausbeute 43 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

Diisopropylazodicarboxylate (97 mg, 0.48 mmol) was added dropwise at r.t. to a solution of (4-chloro-2-methyl-quinolin-7-yl)-methanol (example 2c, 100 mg, 0.48 mmol), triphenylphosphine (126 mg, 0.48 mmol), 2-methoxyphenol (60 mg, 0.48 mmol) in dichloromethane (2.5 mL). After shaking 24 h at r.t., the solvent was evaporated, and the residue was taken up in pyrrolidine (1.37 g, 19.2 mmol) and shaken for 23 h at 80° C. After cooling the reaction mixture was partitioned between sat. aq. ammonium chloride solution and dichloromethane, the organic layer was washed with brine, dried (MgSO4), and evaporated. Chromatography (SiO2, dichloromethane/methanol 19:1) yielded a yellowish solid which was dissolved in ethanol and treated with 20% ethanolic oxalic acid solution. The precipitate was collected by filtration and dried to afford the title compound (90 mg, 43%). Off-white solid, ISP-MS: m/e=349.4 ([M+H—C2H2O4]+).

Aufarbeitung

  1. customthe solvent was evaporated
  2. stirringshaken for 23 h at 80° C
  3. temperatureAfter cooling the reaction mixture
  4. customwas partitioned between sat. aq. ammonium chloride solution and dichloromethane
  5. washthe organic layer was washed with brine
  6. dry with materialdried (MgSO4)
  7. customevaporated
  8. customChromatography (SiO2, dichloromethane/methanol 19:1) yielded a yellowish solid which
  9. filtrationThe precipitate was collected by filtration
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-3460d1419998418fbea719f32b1273b2
Quelldatensatz
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06787558B2

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