Triethylamine → HCID 18784851, compound
Reaction equation
[CH3:1][N:2]([CH3:18])[S:3]([C:6]1[O:7][C:8]2[C:14]([O:15][CH3:16])=[CH:13][CH:12]=[C:11](Br)[C:9]=2[CH:10]=1)(=[O:5])=[O:4].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)CC)C.[O:45]1[CH2:49]CCC1.[OH2:50]>C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl>[CH3:1][N:2]([CH3:18])[S:3]([C:6]1[O:7][C:8]2[C:9](=[C:11]([C:49]([OH:45])=[O:50])[CH:12]=[CH:13][C:14]=2[O:15][CH3:16])[CH:10]=1)(=[O:5])=[O:4]Participants
6
Procedure
Prepared from 4-bromo-7-methoxybenzofuran-2-sulfonic acid dimethylamide (1.0 g), triphenylphosphine (0.28 g), bis(triphenylphosphine)palladium (II) chloride (0.15 g) and triethylamine (4.2 ml) in tetrahydrofuran/water (40 ml/20 ml). The title compound was obtained as a white solid (0.79 g).
Sources & evidence
- ORD record
- ord-665154f59ec048a5936cc78d7d36d306
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06066657
Reaction notes
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