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HRID 43354作成日:2026年10月26日

Methyl isobutyrate → 1,1-Dimethylethyl (2R,6S)-4-({4-[1,1-dimethyl-2-(methyloxy)-2-oxoethyl]phenyl}methyl)-2,6-dimethyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/43354

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl isobutyrateHCID 11039—
反応物Lithium dicyclohexylamideHCID 10932176—
反応物1,1-Dimethylethyl (2R,6S)-4-[(4-bromophenyl)methyl]-2,6-dimethyl-1-piperazinecarboxylateHCID 25224097—
触媒Tris(1,1-dimethylethyl)phosphineHCID 83681—
触媒1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
溶媒TolueneHCID 1140—
生成物1,1-Dimethylethyl (2R,6S)-4-({4-[1,1-dimethyl-2-(methyloxy)-2-oxoethyl]phenyl}methyl)-2,6-dimethyl-1-piperazinecarboxylateHCID 2522420665.5%

反応手順

A solution of methyl 2-methylpropanoate (188 ul, 1.64 mmol) in toluene (3 ml) was added to lithium dicyclohexylamide (362 mg, 1.93 mmol) under glove bag conditions. The suspension was stirred for 10 mins then added to a mixture of D43 (570 mg, 1.49 mmol) and bis(dibenzylideneacetone) palladium (0) (43 mg, 0.074 mmol). Tri(tert-butyl)phosphine (18 ul, 0.074 mmol) was added and the reaction mixture stirred at room temperature overnight. The solvent was removed in vacuo and chromatography eluting with 0-90% EtOAc/petroleum ether gave the title compound as a yellow oil (395 mg). δH (CDCl3, 250 MHz) 7.29 (4H, m), 4.07 (2H, m), 3.66 (3H, s), 3.46 (2H, s), 2.61 (2H, m), 2.12 (2H, dd), 1.58 (6H, s), 1.46 (9H, s), 1.29 (6H, d). MS (ES): MH+ 405.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536182B2
出典データセットuspto-grants-2013_09
ORD IDord-c5561e98662a4bdd91f7af42e78611f5
出典メモuspto-grants-2013_09