Reaktion #9216

ord-1a6875afea914c3fb284eeb3add847f4

Reaktionsgleichung

CCNC(=O)Nc1nc2cccc(S(=O)(=O)C(F)(F)F)c2s1
1-(7-trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylurea
CCN(CC)CC
triethylamine
C#C[Si](C)(C)C
trimethylsilyl acetylene
CCNC(=O)Nc1nc2cccc(C#C[Si](C)(C)C)c2s1
desired compound
Ausbeute 93.0%
CCNC(=O)Nc1nc2cccc(C#C[Si](C)(C)C)c2s1
1-(7-Trimethylsilylacetylenyl-2-benzothiazolyl)-3-ethylurea
Ausbeute 93.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas bubbled with nitrogen gas for 5 minutes
  2. 2
    TemperaturThe mixture was cooled down
  3. 3
    Sonstigeevaporated to dryness
  4. 4
    SonstigePurification by flash chromatography on SiO2 with ethyl acetate and heptane (2/1)

Vorschrift

A mixture of 1-(7-trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylurea (0.080 g, 80% pure, 0.17 mmol), Pd(PPh3)2Cl2 (0.010 g, 0.014 mmol, 0.08 eq), and triethylamine (0.102 mL, 0.73 mmol, 4.3 eq) in 1 mL of anhydrous DMF was bubbled with nitrogen gas for 5 minutes, followed by the addition of trimethylsilyl acetylene (0.12 mL, 0.85 mmol, 5.0 eq). The mixture was heated at about 100° C. with stirring in a sealed tube for about 18 hours. The mixture was cooled down, taken up in 10 mL MeOH, and evaporated to dryness. Purification by flash chromatography on SiO2 with ethyl acetate and heptane (2/1) gave pure desired compound 0.050 g (93%). LC/MS 318 (M+1); LC retention time 9.25 min.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091227B2uspto-grants-2006_08