Pyridine → N-[3-(Bromoacetyl)-2-oxo-1-imidazolidinyl]carbamic acid, 1,1-dimethylethyl ester

HRID 4118Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 4118
[O:1]=[C:2]1[NH:6][CH2:5][CH2:4][N:3]1[NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11].N1C=CC=CC=1.[Br:21][CH2:22][C:23](Br)=[O:24]>ClCCl>[Br:21][CH2:22][C:23]([N:6]1[CH2:5][CH2:4][N:3]([NH:7][C:8](=[O:14])[O:9][C:10]([CH3:11])([CH3:13])[CH3:12])[C:2]1=[O:1])=[O:24]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 61147Bromoacetyl bromideHCID 142789411-[(t-Butoxycarbonyl)amino]-2-imidazolidinone

Produkt 1

HCID 57105682N-[3-(Bromoacetyl)-2-oxo-1-imidazolidinyl]carbamic acid, 1,1-dimethylethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

N-(2-Oxo-1-imidazolidinyl)carbamic acid, 1,1-dimethylethyl ester (12.0 g, 0.06 mmol) was dissolved in dichloromethane (75 ml) containing pyridine (5.2 g, 0.066 mol). The solution was cooled to 0° C. and treated slowly with bromoacetyl bromide (13.3 g, 0.066 mol). The solution was evaporated in vacuo to give a yellow oil. The oil was chromatographed on silica gel (~300 g) eluting with 10% ethyl acetate/dichloromethane. The appropriate fractions were combined and evaporated in vacuo to give the title compound as a white solid, 16.7 g.

Aufarbeitung

  1. customThe solution was evaporated in vacuo
  2. customto give a yellow oil
  3. customThe oil was chromatographed on silica gel (~300 g)
  4. washeluting with 10% ethyl acetate/dichloromethane
  5. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b1182f573e4048b888b6653ec0ae28f6
Quelldatensatz
uspto-grants-1988_02
Patentnummer
US04723002

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