반응 #365196

ord-9d2399faeafc42679852b5a926c327a6

반응 방정식

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CC(C)[Si](C(C)C)(C(C)C)n1cc(C2CCN(C)CC2)c2cc(Br)ccc21
5-bromo-3-(1-methylpiperidin-4-yl)-1-(triisopropylsilyl)-indole
OB(O)c1cc2ccccc2s1
benzo[b]thiophene-2-boronic acid
CN1CCC(c2c[nH]c3ccc(-c4cc5ccccc5s4)cc23)CC1
title compound
CN1CCC(c2c[nH]c3ccc(-c4cc5ccccc5s4)cc23)CC1
5-(Benzo[b]thien-2-yl)-3-(1-Methylpiperidin-4-yl)-1H-Indole
CC(C)[Si](C(C)C)(C(C)C)n1cc(C2CCN(C)CC2)c2cc(-c3cc4ccccc4s3)ccc21
5-(2-benzo[b]thienyl)-3-(1-methylpiperidin-4-yl)-1-(triisopropylsilyl)-indole
수율 40.8%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The title compound was prepared by the procedure of Example 10, beginning with 5-bromo-3-(1-methylpiperidin-4-yl)-1-(triisopropylsilyl)-indole (0.700 g, 1.56 mmol), benzo[b]thiophene-2-boronic acid (0.336 g, 1.87 mmol), tetrakis(triphenylphosphine)palladium(0) (0.090 g, 0.078 mmol), and 2M aqueous sodium carbonate solution (3 mL) in toluene (15 mL) to give 0.160 g of 5-(2-benzo[b]thienyl)-3-(1-methylpiperidin-4-yl)-1-(triisopropylsilyl)-indole (22%) as a solid, which was desilylated by dissolving in 1 mL of tetrahydrofuran and treating with tetrabutylammonium fluoride (1M in tetrahydrofuran, 7 mL) to give the title compound (0.048 g, 43%) as an amorphous solid. FDMS m/e=346 (M+). EA calculated for C22H22N2S.¼ H2O: C, 75.28; H, 6.46; N, 7.98. Found: C, 75.11; H, 6.84; N, 7.91.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06358972B1uspto-grants-2002_03