Sodium Chloride → (R)-2-chloro-N-[1-[(3-chloro-2-thienyl)methyl]propyl]-3-nitro-4-pyridinamine

HRID 1857040Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1857040
[Cl:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[CH2:7][C@H:8]([NH:11][C:12]1[CH:17]=[CH:16][N:15]=[C:14](O)[C:13]=1[N+:19]([O-:21])=[O:20])[CH2:9][CH3:10].CCN(C(C)C)C(C)C.Cl.P(Cl)(Cl)([Cl:34])=O.[Cl-].[Na+]>C1(C)C=CC=CC=1>[Cl:34][C:14]1[C:13]([N+:19]([O-:21])=[O:20])=[C:12]([NH:11][C@@H:8]([CH2:7][C:3]2[S:4][CH:5]=[CH:6][C:2]=2[Cl:1])[CH2:9][CH3:10])[CH:17]=[CH:16][N:15]=1

Komponenten

6

Edukt 4

HCID 5234Sodium ChlorideHCID 24813Phosphorus oxychlorideHCID 10997398Ethylbis(propan-2-yl)amine hydrochlorideHCID 178455879HCID 178455879, Verbindung2×

Produkt 1

HCID 10882512(R)-2-chloro-N-[1-[(3-chloro-2-thienyl)methyl]propyl]-3-nitro-4-pyridinamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

A toluene solution of (R)-N-[1-[(3-chloro-2-thienyl)methyl]propyl]-2-hydroxy-3-nitro-4-pyridinamine (Compound IV) (0.1 mole in 100 mL of toluene) containing 2 equivalents of DIPEA hydrochloride is heated to 60° C. and 20.6 grams of phosphorus oxychloride is added over 10 minutes with stirring. The reaction is stirred at 60° C. until complete (3 hours). After cooling to 0° C., 245 grams of 2N sodium chloride is added at such a rate so as to maintain the reaction temperature below 10° C. The biphasic mixture is stirred 1-2 hours at 0° C. before it is allowed to warm to room temperature overnight. The bottom aqueous layer is separated from the organic layer. The organic layer is concentrated in vacuo and the residue purified by flash chromatography eluting with 25.75 ethyl acetate:heptane to give Compound V. MS (EI) m/z 345 (10%). 1HNMR (500 Mhz, CDCl3 /CD3OD)δ1.0 (2H, t); 1.5-1.8 (2H, m); 2.9-3.2 (2H, m); 3.8 (1H, m); 6.5 (1H, bd); 6.6 (1H, d); 7.15 (1H, d); 7.9 (1H, d).

Aufarbeitung

  1. stirringThe reaction is stirred at 60° C. until complete (3 hours)
  2. temperatureAfter cooling to 0° C.
  3. temperatureto maintain the reaction temperature below 10° C
  4. stirringThe biphasic mixture is stirred 1-2 hours at 0° C. before it
  5. temperatureto warm to room temperature overnight
  6. customThe bottom aqueous layer is separated from the organic layer
  7. concentrationThe organic layer is concentrated in vacuo
  8. customthe residue purified by flash chromatography
  9. washeluting with 25.75 ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-afeab450efc74d08be4464bf402da155
Quelldatensatz
uspto-grants-2000_11
Patentnummer
US06143894

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