Lithium Hydroxide → 2-((2,2,2-Trifluoroethyl)amino)quinoline-7-carboxylic acid

HRID 881004Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 881004
[F:1][C:2]([F:20])([F:19])[CH2:3][NH:4][C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][C:9]([C:15]([O:17]C)=[O:16])=[CH:10][CH:11]=2)[N:6]=1.[OH-].[Li+]>O1CCCC1>[F:20][C:2]([F:1])([F:19])[CH2:3][NH:4][C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][C:9]([C:15]([OH:17])=[O:16])=[CH:10][CH:11]=2)[N:6]=1

Komponenten

4

Edukt 2

HCID 3939Lithium HydroxideHCID 67491717Methyl 2-((2,2,2-trifluoroethyl)amino)quinoline-7-carboxylate

Produkt 1

HCID 674915972-((2,2,2-Trifluoroethyl)amino)quinoline-7-carboxylic acidAusbeute 40 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of methyl 2-((2,2,2-trifluoroethyl)amino)quinoline-7-carboxylate (172 mg, 0.605 mmol) in tetrahydrofuran (5 mL) was added aqueous lithium hydroxide (1.82 mL, 1.82 mmol, 1M solution) at room temperature. The reaction was stirred for 2.5 days. The solvent was removed under reduced pressure and the residue was acidified with 1N aqueous hydrochloric acid. The resulting precipitate was filtered and dried to give the title compound (65 mg, 40%) +ESI (M+H) 271.1, 1H NMR (400 MHz, DMSO-d6, δ): 4.31-4.41 (m, 2H) 7.01 (d, J=8.87 Hz, 1H) 7.69-7.80 (m, 2H) 8.06 (d, J=8.66 Hz, 1H) 8. 14 (s, 1H) 13.03 (bs, 1H)

Aufarbeitung

  1. customThe solvent was removed under reduced pressure
  2. filtrationThe resulting precipitate was filtered
  3. customdried

Quellen und Nachweise

ORD-Eintrag
ord-4b45298a06b2405e91ccda96e20ef5fe
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08993586B2

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