2-(Tri-n-butylstannyl)thiophene → HCID 22031480, compound

HRID 1792442Notes

Reaction equation

HRID 1792442 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][N:6]=[C:5]2Cl.C([Sn](CCCC)(CCCC)[C:18]1[S:19][CH:20]=[CH:21][CH:22]=1)CCC>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][N:6]=[C:5]2[C:18]1[S:19][CH:20]=[CH:21][CH:22]=1

Participants

4

Reactant 2

HCID 27793732-(Tri-n-butylstannyl)thiopheneHCID 167703106-Bromo-4-chloro-quinazoline

Product 1

HCID 22031480HCID 22031480, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Conditions

Temperature
80 °C

Procedure

0.6 g 6-bromo-4-chloroquinazoline was dissolved in 18 mL toluene, and 0.82 mL tri-n-butyl(2-thienyl)stannane and 0.14 g tetrakis (triphenylphosphine)palladium (0) were added thereto and stirred at 80° C. for 24 hours under nitrogen atmosphere. After the solvent was evaporated, the residue was purified by silica gel chromatography (hexane/ethyl acetate), to give 0.29 g of the title compound as yellow crystals.

Workup

  1. customAfter the solvent was evaporated
  2. customthe residue was purified by silica gel chromatography (hexane/ethyl acetate)

Sources & evidence

ORD record
ord-4b79f5dff96f4fe7a29b5ace3d4445d4
Source dataset
uspto-grants-2006_07
Patent number
US07074801B1

Reaction notes

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