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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 331077생성일: 2026년 10월 23일

Isocyanate → HCID 59334017, 화합물

https://huagongshe.com/ko/reaction/331077

반응식

참여 물질

역할이름HCID투입량
반응물IsocyanateHCID 105034—
반응물Tetrahydro-4H-pyran-4-oneHCID 121599—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(2S,5R)-1-Benzyl-2,5-dimethylpiperazineHCID 23402345—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물HCID 59334017HCID 5933401784%

반응 단계

To a mixture of (2S,5R)-1-benzyl-2,5-dimethylpiperazine (11.0 g, 53.8 mmol) and of tetrahydro-4H-pyran-4-one (5.39 g, 53.8 mmol) at 0° C. was added Ti(IV) isopropoxide (19.2 mL, 67.3 mmol). The resulting mixture was stirred at rt overnight and an orange suspension was obtained. To the suspension was added EtOH (25 mL) and NaCNBH3 (4.27 g, 64.6 mmol, 1.20 eq). The resulting mixture was stirred at rt for 24 h. The reaction mixture was then quenched with water (5.0 mL) and a yellow solid was generated. The suspension was diluted with EtOAc (400 mL) and filtered. The filtrate was concentrated under reduced pressure. The residue was again diluted with EtOAc (500 mL), dried over Na2SO4, and filtered. The filtrate was collected and concentrated under reduced pressure to afford a yellow oil. The oil was diluted in THF (400 mL) and PS-isocyanate was added to remove secondary amine. The suspension was filtered and the filtrate concentrated. The residue was purified by column chromatography using 50:5:1 CHCl3/MeOH/Et3N to afford the desired compound as yellow oil (13.0 g, 84%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877761B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-891eeedd9aca48aa80cc2734d6062d6b
출처 메모uspto-grants-2014_11