Indole → HCID 10912416, compound

HRID 1243075Notes

Reaction equation

HRID 1243075 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[CH2:10]([O:12][C:13](=[O:21])[C:14]1[CH:19]=[CH:18][C:17](I)=[CH:16][CH:15]=1)[CH3:11].[O-]P([O-])([O-])=O.[K+].[K+].[K+].CN[C@@H]1CCCC[C@H]1NC>[Cu]I.C1(C)C=CC=CC=1>[CH2:10]([O:12][C:13]([C:14]1[CH:19]=[CH:18][C:17]([N:1]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[CH:3]=[CH:2]2)=[CH:16][CH:15]=1)=[O:21])[CH3:11]

Participants

7

Reactant 4

HCID 798IndoleHCID 62657Potassium Phosphate, TribasicHCID 142891Ethyl 4-iodobenzoateHCID 2733821trans-N,N'-dimethyl-1,2-cyclohexanediamine

Product 1

HCID 10912416HCID 10912416, compound

Reagents, catalysts & solvents 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)CatalystHCID 1140TolueneSolvent

Procedure

Using the general procedure, indole (0.117 g, 1.00 mmol) was coupled at 80° C. with ethyl-4-iodobenzoate (0.331 g, 1.20 mmol) using CuI (9.5 mg, 0.050 mmol, 5.0 mol %), K3PO4 (2.1 mmol), trans-N,N′-dimethyl-1,2-cyclohexanediamine (32 μL, 0.20 mmol, 20 mol %) and toluene (1.0 mL) to give the crude product. The above product was identified by comparison (GC) to a previously prepared sample and the GC yield was determined to be 96%.

Sources & evidence

ORD record
ord-566eace04e4e4d8aad66e3e7d029243d
Source dataset
uspto-grants-2006_10
Patent number
US07115784B2

Reaction notes

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