تفاعل #52418
ord-e5c46863350e440095e86e1636b8d707
معادلة التفاعل
1-ethynyl-4-(1-methoxycyclopropyl)-benzene
4-(1-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-6-ylethynyl)-benzoic acid ethyl ester
Intermediate 61
4-(1-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-6-ylethynyl)-benzoic acid ethyl ester
methyl-(4-iodophenyl)-acetate
4-iodo phenyl acetic acid methyl ester
Reagent B
4-iodo phenyl acetic acid methyl ester
triethyl amine
→
المتفاعلات
1-ethynyl-4-(1-methoxycyclopropyl)-benzene
4-(1-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-6-ylethynyl)-benzoic acid ethyl ester
Intermediate 61
4-(1-cyclopropyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-6-ylethynyl)-benzoic acid ethyl ester
methyl-(4-iodophenyl)-acetate
4-iodo phenyl acetic acid methyl ester
Reagent B
4-iodo phenyl acetic acid methyl ester
triethyl amine
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىsparged with argon for 5 minutes
الإجراء التجريبي
Using General Procedure F; 1-ethynyl-4-(1-methoxycyclopropyl)-benzene (Intermediate 61, 120.0 mg, 0.56 mmol) and methyl-(4-iodophenyl)-acetate (Reagent B, 154.0 mg, 0.56 mmol) in triethyl amine (6 mL) was treated with copper(I)iodide (35.0 mg, 0.19 mmol) and sparged with argon for 5 minutes. Dichlorobis(triphenylphosphine)palladium(II) (130 mg, 0.19 mmol) was added and the reaction mixture was stirred overnight at room temperature. Column chromatography (2-8% EtOAc—hexanes) afforded 140.0 mg (78%) of the title compound as an orange solid.