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HRID 2428172作成日:2026年10月25日

Ammonium Chloride → (rac.)-(1R*,5S*)-7-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-9-methyl-3,9-diaza-bicyclo[3.3.1]non-7-ene-3,6-dicarboxylic Acid 3-tert-butyl Ester 6-ethyl Ester

https://huagongshe.com/reaction/2428172

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物(4-Bromophenoxy)(tert-butyl)dimethylsilaneHCID 4227167—
反応物(rac.)-(1R*,5S*)-9-Methyl-7-trifluoromethanesulfonyloxy-3,9-diaza-bicyclo[3.3.1]non-6-ene-3,6-dicarboxylic acid 3-tert-butyl ester 6-ethyl esterHCID 44158352—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物(rac.)-(1R*,5S*)-7-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-9-methyl-3,9-diaza-bicyclo[3.3.1]non-7-ene-3,6-dicarboxylic Acid 3-tert-butyl Ester 6-ethyl EsterHCID 13172896883%

反応条件

温度-78 °C

反応手順

BuLi (1.6M in hexane, 31.9 mL, 51.0 mmol) was added to a sol. of (4-bromo-phenoxy)-tert-butyl-dimethyl-silane (12.8 g, 44.5 mmol) in THF (150 mL) at −78° C. The mixture was stirred for 60 min at −78° C., and ZnCl2 (1.1M, 50.5 mL, 55.6 mmol) was added. The mixture was allowed to warm to rt, and a sol. of (rac.)-(1R*,5S*)-9-methyl-7-trifluoromethanesulfonyloxy-3,9-diaza-bicyclo[3.3.1]non-6-ene-3,6-dicarboxylic acid 3-tert-butyl ester 6-ethyl ester (WO 2003/093267; 17.0 g, 37.1 mmol) in THF (10 mL) and Pd(PPh3)4 (1.07 g, 0.927 mmol) were added. The mixture was stirred at 50° C. for 25 min, and was allowed to cool to rt. Aq. sat. NH4Cl was added, and the mixture was extracted with EtOAc (3×). The combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (EtOAc/heptane 6:4) yielded the title compound (15.9 g, 83%). LC-MS: tR=0.95 min, ES+: 517.25.

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-3fbf09bb370849cca25ee48ea702dd54
出典メモuspto-grants-2011_06