تفاعل #470384

ord-d362b76ab07f4a969319ee953df8d0c5

معادلة التفاعل

Brc1ccc(Br)nc1
2,5-dibromo-pyridin
CC1(C)OB(c2cnc3ccccc3c2)OC1(C)C
3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-quinoline
O=C([O-])[O-].[K+].[K+]
K2CO3
C1CCOC1
THF
Brc1ccc(-c2cnc3ccccc3c2)nc1
white solid
المردود 107.4%
Brc1ccc(-c2cnc3ccccc3c2)nc1
3-(5-bromo-pyridin-2-yl)-quinoline
المردود 107.4%

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added
  2. 2
    استخلاصthe mixture was subject to extraction
  3. 3
    استخلاصThen, an organic layer extracted
  4. 4
    أخرىtherefrom was dried
  5. 5
    ترشيحfiltered
  6. 6
    أخرىA solvent was removed
  7. 7
    أخرىthe resultant was separated

الإجراء التجريبي

1.1 g (4.7 mmol) of 2,5-dibromo-pyridin, 1.0 g (3.92 mmol) of 3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-quinoline, 0.45 g of tetrakis(triphenylphosphine)palladium(0), 7.84 ml of 2M K2CO3 and 1.26 g of tetrabutylammoniumbromide were added to a 100 ml round-bottom flask in an argon atmosphere, and 30 ml of THF and 15 ml of toluene were added thereto. Then, the mixture was refluxed at 100° C. for 16 hours. When the mixture solution turned dark brown, water was added thereto and the mixture was subject to extraction using chloroform. Then, an organic layer extracted therefrom was dried using anhydrous magnesium sulfate and filtered. A solvent was removed and the resultant was separated using a silica gel column chromatography to obtain 1.2 g of white solid 3-(5-bromo-pyridin-2-yl)-quinoline which was identified by APCI using LCMS. As a result, a main peak was observed at [M+H]+=285.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08367219B2uspto-grants-2013_02