Hydrochloric Acid → 8-(2-Amino-6-methylbenzylamino)-3-chloro-2-methylimidazo[1,2-a]pyridine hydrochloride

HRID 1955013Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1955013
[N+:1]([C:4]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:23])[C:5]=1[CH2:6][NH:7][C:8]1[C:9]2[N:10]([C:14]([Cl:18])=[C:15]([CH3:17])[N:16]=2)[CH:11]=[CH:12][CH:13]=1)([O-])=O.Cl>CO.O1CCOCC1.[Pt]>[ClH:18].[NH2:1][C:4]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:23])[C:5]=1[CH2:6][NH:7][C:8]1[C:9]2[N:10]([C:14]([Cl:18])=[C:15]([CH3:17])[N:16]=2)[CH:11]=[CH:12][CH:13]=1

Komponenten

6

Edukt 2

HCID 313Hydrochloric AcidHCID 232941638-(2-Nitro-6-methylbenzylamino)-3-chloro-2-methylimidazo[1,2-a]pyridine

Produkt 1

HCID 232941698-(2-Amino-6-methylbenzylamino)-3-chloro-2-methylimidazo[1,2-a]pyridine hydrochlorideAusbeute 164,1 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23939PlatinumKatalysatorHCID 887MethanolLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

A solution of 8-(2-nitro-6-methylbenzylamino)-3-chloro-2-methylimidazo[1,2-a]pyridine (2.0 g, 6 mmol) in methanol (175 ml) and dioxane (175 ml) is treated with platinum-on-carbon catalyst (5% strength) and hydrogenated at RT under atmospheric pressure for 2 h. After 2 h, 2N hydrochloric acid (5 ml) is added and the mixture is hydrogenated under the same conditions again for 1 h. The catalyst is then filtered off, the filtrate is adjusted to pH 8.5 using 2N sodium hydroxide solution and the solvent is distilled off on a rotary evaporator. The residue is dissolved in boiling ethyl acetate (400 ml). After cooling to RT, diisopropyl ether (250 ml) is added and, to complete crystallization, the mixture is stirred at 4° C. for 30 min. The precipitate is then filtered off with suction, washed with diisopropyl ether and dried in vacuo. The title compound (1.66 g, 92%) is isolated as a beige solid. M.p. 243-246° C.

Aufarbeitung

  1. waitthe mixture is hydrogenated under the same conditions again for 1 h
  2. filtrationThe catalyst is then filtered off
  3. distillationthe solvent is distilled off on a rotary evaporator
  4. dissolutionThe residue is dissolved
  5. additiondiisopropyl ether (250 ml) is added
  6. customcrystallization
  7. filtrationThe precipitate is then filtered off with suction
  8. washwashed with diisopropyl ether
  9. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-933a7b0e940a4e67bf906576e223b40b
Quelldatensatz
uspto-grants-2000_09
Patentnummer
US06124313

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