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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43354생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl isobutyrateHCID 11039—
반응물Lithium dicyclohexylamideHCID 10932176—
반응물1,1-Dimethylethyl (2R,6S)-4-[(4-bromophenyl)methyl]-2,6-dimethyl-1-piperazinecarboxylateHCID 25224097—
촉매Tris(1,1-dimethylethyl)phosphineHCID 83681—
촉매1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
용매TolueneHCID 1140—
생성물1,1-Dimethylethyl (2R,6S)-4-({4-[1,1-dimethyl-2-(methyloxy)-2-oxoethyl]phenyl}methyl)-2,6-dimethyl-1-piperazinecarboxylateHCID 2522420665.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536182B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c5561e98662a4bdd91f7af42e78611f5
출처 메모uspto-grants-2013_09