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Propylamine → 2-Amino-5-iodo-N-propylbenzamide

HRID 1276620
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1276620
[CH2:1]([NH2:4])[CH2:2][CH3:3].[I:5][C:6]1[CH:7]=[CH:8][C:9]2[NH:14]C(=O)O[C:11](=[O:16])[C:10]=2[CH:17]=1>N1C=CC=CC=1>[NH2:14][C:9]1[CH:8]=[CH:7][C:6]([I:5])=[CH:17][C:10]=1[C:11]([NH:4][CH2:1][CH2:2][CH3:3])=[O:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 7852PropylamineHCID 2944806-iodo-2H-3,1-benzoxazine-2,4(1H)-dione

Produkt 1

HCID 221165242-Amino-5-iodo-N-propylbenzamideAusbeute 74,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

Propylamine (1.2 g, 20.3 mmol) and 6-iodo-2H-3,1-benzoxazine-2,4(1H)-dione (5.0 g, 17.3 mmol) were combined in pyridine (85 mL) and stirred at room temperature for 24 h. The reaction was concentrated under reduced pressure and the resulting residue was partitioned between ethyl acetate (200 mL) and 5% hydrochloric acid (200 mL). The phases were separated and the organic phase was washed with 1N sodium hydroxide, water, and brine. Drying over anhydrous sodium sulfate and evaporation under reduced pressure afforded 3.9 g of the title compound, 1H NMR (300 MHz, CDCl3): δ0.99 (t,3H1); 1.63 (m,2H); 3.35 (m,2H); 5.52 (br s,2H); 5.95 (br s,1H); 6.47 (d, 1H); 7.42 (dd,1H); 7.55(d,1H).

Aufarbeitung

  1. concentrationThe reaction was concentrated under reduced pressure
  2. customthe resulting residue was partitioned between ethyl acetate (200 mL) and 5% hydrochloric acid (200 mL)
  3. customThe phases were separated
  4. washthe organic phase was washed with 1N sodium hydroxide, water, and brine
  5. dry with materialDrying over anhydrous sodium sulfate and evaporation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-ba8aa42850ad44af9b79907d0b0c5476
Quelldatensatz
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06166208

Notizen zur Reaktion

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