Tetrahydrofuran → 1-Cyclopropyl-6-ethynyl-4,4-dimethyl-1,2,3,4-tetrahydroquinoline

HRID 1069889Notes

Reaction equation

HRID 1069889 reaction equation
COC(=O)C1C=CC(C#C[C:12]2[CH:13]=[C:14]([CH:26]3[CH2:28]C3)[C:15]3O[C:19]4(CC4)[CH2:18][C:17]([CH3:24])([CH3:23])[C:16]=3[CH:25]=2)=CC=1F.C(O[C:34](=O)[C:35]1[CH:40]=CC(I)=CC=1)C.C([N:45](CC)CC)C.O1CCCC1>CCCCCC.[Cu]I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(OCC)(=O)C>[CH:35]1([N:45]2[C:25]3[C:16](=[CH:15][C:14]([C:26]#[CH:28])=[CH:13][CH:12]=3)[C:17]([CH3:23])([CH3:24])[CH2:18][CH2:19]2)[CH2:34][CH2:40]1

Participants

9

Procedure

Following general procedure F and using 1-cyclopropyl-6-ethynyl-4,4-dimethyl-1,2,3,4-tetrahydro quinoline (Intermediate 53, 0.11 g, 0.43 mmol), ethyl-4-iodo-benzoate (Reagent A, 0.11 g, 0.9 mmol), triethyl amine (3 mL), tetrahydrofuran(3 mL), copper(I)iodide (0.02 g, 0.1 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.060 g, 0.085 mmol) followed by flash column chromatography over silica gel (230-400 mesh) using 5-10% ethyl acetate in hexane as the eluent, the title compound was obtained (0.05 g, 31%).

Sources & evidence

ORD record
ord-3a8f26fc804b49ec84cb7bc22bfc1245
Source dataset
uspto-grants-2001_06
Patent number
US06252090B1

Reaction notes

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