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HRID 2105029作成日:2026年10月27日

Pentamethyldiethylenetriamine → (4-bromo-1-trityl-1H-imidazol-2-yl)(3-chloro-5-ethyl-2-fluorophenyl)methanol

https://huagongshe.com/reaction/2105029

反応式

関与物質

役割名称HCID仕込み量
反応物PentamethyldiethylenetriamineHCID 18196—
反応物2-Chloro-4-ethyl-1-fluorobenzeneHCID 18711878—
反応物4-bromo-1-trityl-1H-imidazole-2-carbaldehydeHCID 86247220—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(4-bromo-1-trityl-1H-imidazol-2-yl)(3-chloro-5-ethyl-2-fluorophenyl)methanolHCID 6881625285,857.703%

反応条件

温度-40 °C

反応手順

To a solution of Intermediate 221.1 (100 mg, 0.631 mmol) and PMDTA (0.15 mL) in 5 mL THF at −70° C., was added BuLi (1.4 M in hexanes, 0.473 mL, 0.662 mmol). The mixture was stirred with warming to −40° C. over 30 min, recooled to −70° C., then a solution of Intermediate 175.1 (263 mg, 0.631 mmol) in 2 mL THF was added. The mixture was slowly warmed to −20° C. over 1 h. The reaction was quenched with sat. NH4Cl, then was diluted with EtOAc. The organic phase was washed with H2O (2×) and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 40% EtOAc/hexanes gradient) to afford 312 g of Intermediate 221.2 as a colorless solid. LCMS (50 to 100% B, 4 min gradient, A=95% H2O/5% CH3CN/0.1% TFA, B=5% H2O/95% CH3CN/0.1% TFA) RT=5.45 min, 575.28 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07576098B2
出典データセットuspto-grants-2009_08
ORD IDord-3cfa38135adf4a4b9a61ce3eb6ddf110
出典メモuspto-grants-2009_08