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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277777생성일: 2026년 10월 25일

Tetrahydrofuran → 1-(1-(4-Cyanobenzyl)imidazole-5-ylmethyl)-4-(tert-butyloxycarbonyl)-(trans)2,5-dimethylpiperazine

https://huagongshe.com/reaction/277777

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-[(5-Formylimidazol-1-yl)methyl]benzonitrileHCID 10632289—
반응물(2R,5S)-2,5-Dimethyl-piperazine-1-carboxylic acid tert-butyl esterHCID 24903576—
촉매Titanium isopropoxideHCID 11026—
용매EthanolHCID 702—
용매Methanol--water (1/1)HCID 22242641—
생성물1-(1-(4-Cyanobenzyl)imidazole-5-ylmethyl)-4-(tert-butyloxycarbonyl)-(trans)2,5-dimethylpiperazineHCID 70153172—

반응 조건

온도60 °C

반응 단계

To a round bottom flask were added 1-(4-cyanobenzyl)-5-formylimidazole (250.0 mg, 1.2 mmole) along with titanium(IV)isopropoxide (1.0 ml, 3.65 mmol), (trans) 2,5-Dimethyl-4-tertbutyloxycarbonylpiprizine (253.7 mg, 1.2 mmol) (prepared as described in Step 1), and tetrahydrofuran (0.4 ml). The reaction was heated at 60° C. for 1.25 hour. The reaction was cooled and sodiumcyanoborohydride (95.0 mg, 1.5 mmol) was added along with ethanol (0.5 ml) and the reaction was stirred at RT for 18 hours. The reaction was diluted with methanol/water (3 ml/1 ml) and the mixture filtered through celite. The filtrate was then concentrated to an oil, dissolved into methanol and put through a High Pressure Liquid Chromatography column. The desired fractions were collected, concentrated, and lyophilized to give the ditrifluoroacetic acid salt of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06358956B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-746d9af315ab4fb7a69c9a5a5da08560
출처 메모uspto-grants-2002_03