Urea → HCID 22672523, Verbindung

HRID 47964

Reaktionsgleichung

Reaktionsgleichung von HRID 47964
[Cl:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[CH:5][C:3]=1[NH2:4].Cl[N:13]([N+]([O-])=O)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.N([O-])=O.[Na+].NC(N)=O.[OH:31][CH2:32][CH2:33][CH2:34][N:35](C1C=CC=CC=1)[CH2:36][CH2:37][CH2:38][C:39]([O:41][CH2:42][CH3:43])=[O:40].C([O-])(=O)C.[Na+]>O.C(O)(=O)C>[Cl:1][C:2]1[CH:8]=[C:7]([N+:9]([O-:11])=[O:10])[CH:6]=[CH:5][C:3]=1[N:4]=[N:13][C:14]1[CH:19]=[CH:18][C:17]([N:35]([CH2:34][CH2:33][CH2:32][OH:31])[CH2:36][CH2:37][CH2:38][C:39]([O:41][CH2:42][CH3:43])=[O:40])=[CH:16][CH:15]=1

Komponenten

9

Edukt 6

HCID 1176UreaHCID 84922-Chloro-4-nitroanilineHCID 517045Sodium AcetateHCID 23668193Sodium NitriteHCID 44144434N-Chloro-N-phenylnitramideHCID 66716979HCID 66716979, Verbindung

Produkt 1

HCID 22672523HCID 22672523, VerbindungAusbeute 68 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 176Acetic AcidLösungsmittelHCID 962WaterLösungsmittel3×

Versuchsvorschrift

2-Chloro-4-nitroaniline 2.5 g (10 mmol) is placed into a 125 mL flask and 6 mL of water is added. Agitation and sonication partially dissolves the yellow chloronitroaniline. Then the stirred solution is cooled with ice in a fume hood and 15.8 mL of concentrated (˜12 M) HCl is added. Most of the yellow material dissolves at this point. The flask is fitted with a dropping funnel, and a solution of 1.51 g (21.9 mmol) sodium nitrite in 3-4 mL of water is added to the dropping funnel and slowly added to the solution in the flask with stirring, over about 20 minutes. When this is complete, 0.6 g (˜21 mmol) of urea is added followed by 2.73 g of ethyl 4-[(3-hydroxypropyl)phenylamino]butanoate as a solution in 8.2 mL acetic acid. After a minute 20 g of sodium acetate in ˜50 mL of water is added. The mixture is allowed to stir for an hour at room temperature. Most of the product is separated as an emulsion. The mixture is partitioned between ethyl acetate and water. The organic layer is washed with NaHCO3 (3×50 ml), brine and dried over anhydrous sodium sulfate. Then the organic solvents are evaporated to a syrup. The crude product is chromatographed on silica gel (1.5×20 inches) eluting with 50% ethyl acetate/hexane. The appropriate fractions are collected, combined, evaporated (30-40 degrees), and dried in a vacuum. The product is a dark oil. The yield is approximately 68-70%. 1H NMR (DMSO-d6) δ: 8.42 (d, J=2.5 Hz, aromatic proton, 1H), 8.24 (dd, J1=9 Hz, J2=2.5 Hz, aromatic proton, 1H), 7.86 (d, J=9 Hz, 2H), 7.77 (d, J=9 Hz, 1H), 6.92 (d, J=9 Hz, aromatic protons, 2H), 4.67 (t, J=6 Hz, OH,1H), 4.07 (q, J=7 Hz, CH2O, 2H), 3.5 (m, aliphatic protons, 6H), 2.40 (t, J=7 Hz, aliphatic protons, 2H), 1.84 (m, aliphatic protons, 2H), 1.72 (m, aliphatic protons, 2H), 1.18 (t, J=7 Hz, CH3, 3H).

Aufarbeitung

  1. customAgitation and sonication
  2. temperatureThen the stirred solution is cooled with ice in a fume hood and 15.8 mL
  3. concentrationof concentrated (˜12 M) HCl
  4. additionis added
  5. dissolutionMost of the yellow material dissolves at this point
  6. customThe flask is fitted with a dropping funnel
  7. additionslowly added to the solution in the flask
  8. stirringto stir for an hour at room temperature
  9. customMost of the product is separated as an emulsion
  10. customThe mixture is partitioned between ethyl acetate and water
  11. washThe organic layer is washed with NaHCO3 (3×50 ml), brine
  12. dry with materialdried over anhydrous sodium sulfate
  13. customThen the organic solvents are evaporated to a syrup
  14. customThe crude product is chromatographed on silica gel (1.5×20 inches)
  15. washeluting with 50% ethyl acetate/hexane
  16. customThe appropriate fractions are collected
  17. customevaporated (30-40 degrees)
  18. customdried in a vacuum

Quellen und Nachweise

ORD-Eintrag
ord-0136e8f0947b46f4903c697b1435d4a8
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06699975B2

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