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HRID 2428187作成日:2026年10月27日

5-Bromo-2-(2-(2,6-dichloro-4-methylphenoxy)ethoxy)pyridine → (rac.)-(1R*,5S*)-3-{6-[2-(2,6-Dichloro-4-methyl-phenoxy)-ethoxy]-pyridin-3-yl}-8-aza-bicyclo[3.2.1]oct-2-ene-2,8-dicarboxylic Acid 8-tert-butyl Ester 2-methyl Ester

https://huagongshe.com/reaction/2428187

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-(2-(2,6-dichloro-4-methylphenoxy)ethoxy)pyridineHCID 44816668—
反応物(rac.)-(1R*,5S*)-3-Trifluoromethanesulfonyloxy-8-aza-bicyclo[3.2.1]oct-2-ene-2,8-dicarboxylic Acid 8-tert-butyl Ester 2-methyl EsterHCID 131728966—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物(rac.)-(1R*,5S*)-3-{6-[2-(2,6-Dichloro-4-methyl-phenoxy)-ethoxy]-pyridin-3-yl}-8-aza-bicyclo[3.2.1]oct-2-ene-2,8-dicarboxylic Acid 8-tert-butyl Ester 2-methyl EsterHCID 13172897778.3%

反応条件

温度-78 °C

反応手順

BuLi (1.6 M in hexane, 12.0 mL, 19.2 mmol) was added to the sol. of 5-bromo-2-[2-(2,6-dichloro-4-methyl-phenoxy)-ethoxy]-pyridine (5.45 g, 14.4 mmol) in THF (120 mL) at −78° C. The mixture was stirred at −78° C. for 60 min, and ZnCl2 (1M in THF, 28.9 mL, 28.9 mmol) was added. The mixture was allowed to warm up to rt, and compound A1 (4.00 g, 9.63 mmol) in dry THF (50 mL) and Pd(PPh3)4 (277 mg, 0.240 mmol) in THF (2 mL) were added. The mixture was heated to 70° C. for 1 h, and was quenched with aq. sat. NH4Cl (70 mL). The mixture was extracted with EtOAc (3×). The combined org. layers were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of crude by FC(CH2Cl2/MeOH 99:1→98:2→97:3→96:4→95:5) yielded the title compound (4.25 g, 78%). LC-MS: tR=1.16 min; ES+: 563.11.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07968720B2
出典データセットuspto-grants-2011_06
ORD IDord-50de53571be8418896785652447dc2da
出典メモuspto-grants-2011_06