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HRID 1487445作成日:2026年10月25日

Triethylamine → Methyl 4-((4S,5R)-3-(2,2-dichloroacetyl)-4-(fluoro-methyl)-2,2-dimethyloxazolidin-5-yl)benzoate

https://huagongshe.com/reaction/1487445

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
反応物(4S,5R)-3-(dichloroacetyl)-4-(fluoromethyl)-5-(4-iodophenyl)-2,2-dimethyl-1,3-oxazolidineHCID 86695394—
反応物HCID 178418416HCID 178418416—
触媒palladium(II) acetateHCID 167845—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物Methyl 4-((4S,5R)-3-(2,2-dichloroacetyl)-4-(fluoro-methyl)-2,2-dimethyloxazolidin-5-yl)benzoateHCID 86695393—

反応条件

温度60 °C

反応手順

To a flask containing 2,2-dichloro-1-((4S,5R)-4-(fluoromethyl)-5-(4-iodophenyl)-2,2-dimethyloxazolidin-3-yl)ethanone (2.0 g, 4.48 mmol) is added triethylamine (5 mL) and methanol (5 mL). Carbon monoxide gas is bubbled through the solution while stirring for 30 min. Pd(OAc)2 (51 mg, 0.22 mmol) and Xantphos (132 mg, 0.22 mmol) are next added and a balloon containing carbon monoxide is secured to the flask outlet. The reaction is heated for 2 hours at 60° C. and then cooled to room temperature. Next, the reaction is diluted with water, extracted with ethylacetate, dried over Na2SO4, and concentrated under vacuum. The residue is chromatographed on silica gel eluting from 100% hexanes to 50:50 ethylacetate:hexanes to afford the title compound (1.11 g): 1H NMR (400 MHz, CDCl3) 8.10 (d, 2H, J=8.0 Hz), 7.55 (d, 2H, J=8.0 Hz), 6.34 (m, 1H), 5.30-4.42 (m, 4H), 3.95 (s, 3H), 1.97-1.53 (m, 6H). m/z (CI) 320 [M-(CH3)2CO].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09428528B2
出典データセットuspto-grants-2016_08
ORD IDord-7616ce6901824690bb5196d5945d06da
出典メモuspto-grants-2016_08