Hydrochloric Acid → 3-Ethyl-5-(1H-indol-3-ylmethyl)-imidazolidine-2,4-dione

HRID 1098618Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1098618
Cl.CO[C:4](=[O:17])[C@H:5]([CH2:7][C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[NH:10][CH:9]=1)[NH2:6].C(N(CC)CC)C.[CH2:25]([N:27]=[C:28]=[O:29])[CH3:26].Cl>ClCCl.O1CCOCC1>[CH2:25]([N:27]1[C:4](=[O:17])[CH:5]([CH2:7][C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=2)[NH:6][C:28]1=[O:29])[CH3:26]

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 8022Ethyl isocyanateHCID 8471TriethylamineHCID 2734891Methyl tryptophanate hydrochloride

Produkt 1

HCID 138140423-Ethyl-5-(1H-indol-3-ylmethyl)-imidazolidine-2,4-dioneAusbeute 93,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

To a solution of L-tryptophan methyl ester hydrochloride (0.510 mg, 0.002 mol.) in dichloromethane (10 mL) was added triethyl amine (0.350 mL, 0.0025 mol.) followed by ethylisocyanate (0.198 mL, 0.0025 mol.). The reaction mixture was stirred at room temperature for 24 hr, and then concentrated. The residue obtained was diluted with dioxane (10 mL) and then conc. HCl (5 mL) was added. The mixture was heated at reflux for 3-4 hr. The reaction mixture was extracted in ethyl acetate, washed with water, dried and concentrated. The residue was purified by column chromatography on silica gel using 60% ethyl acetate-hexane to give 893-04 (480 mg, 93%): mp 167-170° C. (lit. 163-164° C.), 1H NMR (400 MHz, CDCl3): 0.99 (t, J=6.8 Hz, 3H), 2.95-3.01 (dd, J=8.4 and 14.8 Hz, 1H), 3.34-3.46 (m, 3H), 4.19-4.22 (dd, J=3.6 and 8.8 Hz, 1H), 5.70 (s, 1H), 6.98 (d, J=2.0 Hz, 1H), 7.06-7.10 (dd, J=8.0 and 6.8 Hz, 1H), 7.16 (dd, J=7.2 and 6.8 Hz, 1H), 7.30 (d, J=8.4 Hz, 1H), 7.55 (d, J=8.8 Hz, 1H), 8.18 (s, 1H).

Aufarbeitung

  1. concentrationconcentrated
  2. customThe residue obtained
  3. temperatureThe mixture was heated
  4. temperatureat reflux for 3-4 hr
  5. extractionThe reaction mixture was extracted in ethyl acetate
  6. washwashed with water
  7. customdried
  8. concentrationconcentrated
  9. customThe residue was purified by column chromatography on silica gel using 60% ethyl acetate-hexane

Quellen und Nachweise

ORD-Eintrag
ord-05828940e6ff4729aec6e11411c137ed
Quelldatensatz
uspto-grants-2012_03
Patentnummer
US08143300B2

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