Реакция #6869

ord-0e8fc914af534bad8676cf7b7037aa71

Уравнение реакции

COc1ccccc1-c1cn2c(n1)C(CCO)N(C(=O)OC(C)(C)C)CC2
product
COc1ccccc1-c1cn2c(n1)C(CCO)N(C(=O)OC(C)(C)C)CC2
7-((1,1-Dimethylethoxy)carbonyl)-8-(2-hydroxyethyl)-2-(2-methoxyphenyl)-5,6,7,8-tetrahydro-imidazo[1,2-a]pyrazine
CCOC(=O)/N=N/C(=O)OCC
Diethylazodicarboxylate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
Triphenylphosphine
SC(c1ccccc1)(c1ccccc1)c1ccccc1
triphenylmethanethiol
COc1ccccc1-c1cn2c(n1)C(CCSC(c1ccccc1)(c1ccccc1)c1ccccc1)N(C(=O)OC(C)(C)C)CC2
foam
Выход 111.0%
COc1ccccc1-c1cn2c(n1)C(CCSC(c1ccccc1)(c1ccccc1)c1ccccc1)N(C(=O)OC(C)(C)C)CC2
7-((1,1-Dimethylethoxy)carbonyl)-2-(2-methoxyphenyl)-5,6,7,8-tetrahydro-8-(2-((triphenylmethyl)thio)ethyl)-imidazo[1,2-a]pyrazine
Выход 111.0%

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas maintained at about <3° C
  2. 2
    workup.STIRRINGThe resulting mixture was stirred for about 1 hour at about 0° C.
  3. 3
    Другоеto warn to room temperature
  4. 4
    КонцентрированиеThe mixture was concentrated under reduced pressure
  5. 5
    workup.DISSOLUTIONthe residue dissolved in ether (40 ml)
  6. 6
    workup.WAITto stand overnight
  7. 7
    ФильтрацияThe solid was filtered off
  8. 8
    Концентрированиеthe filtrate was concentrated
  9. 9
    Другоеthen purified by flash chromatography on silica gel using 4:1/hexanes
  10. 10
    Концентрированиеconcentrated under reduced pressure

Методика

Triphenylphosphine (4.08 g, 15.5 mmol) was dissolved in THF (25 ml), cooled to about 0° C. under N2 and Diethylazodicarboxylate (2.45 ml, 15.54 mmol) was added at a dropwise rate so that the reaction temperature was maintained at about <3° C. Stirring was continued for about ½ hour at 0° C. A mixture of the triphenylmethanethiol (4.30 g, 15.54 mmol) and the product from Step 13.e. (2.90 g, 7.77 mmol) in THF (25 ml) was added at a dropwise rate. The resulting mixture was stirred for about 1 hour at about 0° C. and then allowed to warn to room temperature. The mixture was concentrated under reduced pressure and the residue dissolved in ether (40 ml) and allowed to stand overnight. The solid was filtered off and the filtrate was concentrated then purified by flash chromatography on silica gel using 4:1/hexanes:EtOAc and then 4:1/hexanes:EtOAc as eluants. The product fractions were combined and concentrated under reduced pressure to obtain a pale yellow foam (5.49 g, 111%) which was used without further purification. Mass spec. 632.4 MH+.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07084135B1uspto-grants-2006_08