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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61501생성일: 2026년 10월 24일

Hydroxylamine → (1S,2S,5R)-N-hydroxy-2-[(4-phenylpiperazin-1-yl)carbonyl]-5-(pyridin-3-ylmethoxy)cyclohexanecarboxamide

https://huagongshe.com/ko/reaction/61501

반응식

참여 물질

역할이름HCID투입량
반응물HydroxylamineHCID 787—
반응물MethanolHCID 887—
반응물3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
반응물Potassium tert-butoxideHCID 23665647—
반응물methyl(1S,2S,5R)-5-hydroxy-2-[(4-phenylpiperazin-1-yl)carbonyl]cyclohexanecarboxylateHCID 67304253—
반응물methyl(1S,2S,5R)-2-[(4-phenylpiperazin-1-yl)carbonyl]-5-(pyridin-3-ylmethoxy)cyclohexanecarboxylateHCID 67305585—
용매TetrahydrofuranHCID 8028—
생성물(1S,2S,5R)-N-hydroxy-2-[(4-phenylpiperazin-1-yl)carbonyl]-5-(pyridin-3-ylmethoxy)cyclohexanecarboxamideHCID 86598268—

반응 단계

1.00 M of Potassium tert-butoxide in tetrahydrofuran (0.212 mL) was added to a mixture of methyl(1S,2S,5R)-5-hydroxy-2-[(4-phenylpiperazin-1-yl)carbonyl]cyclohexanecarboxylate (36.8 mg, 0.000106 mol) and 3-chloromethylpyridine hydrochloride (17.4 mg, 0.106 mmol) in tetrahydrofuran (1.0 mL, 0.012 mol) at 0 Celsius. The mixture was stirred at room temperature for 1 hr then purified by HPLC. 1.5 M of hydroxyamine solution (0.7 ml) was added into to a solution of methyl(1S,2S,5R)-2-[(4-phenylpiperazin-1-yl)carbonyl]-5-(pyridin-3-ylmethoxy)cyclohexanecarboxylate (0.075 mmol, 0.000075 mol) made above in methanol (0.5 mL, 0.01 mol). It was stirred at rt for 2 hrs then purified by Prep-HPLC.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440958B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-7d23e9155f67488ea69ffa1c4a4e0b7d
출처 메모uspto-grants-2016_09