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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1177724생성일: 2026년 10월 27일

Hydrochloric Acid → 1-[1,4']Bipiperidinyl-1'-yl-2-(di-tert-butoxycarbonylamino)-3-(4-hydroxy-piperidin-1-yl)-propan-1-one

https://huagongshe.com/reaction/1177724

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,4'-BipiperidineHCID 78607—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물2-(Di-tert-butoxycarbonylamino)-3-(4-hydroxy-piperidin-1-yl)-propionic acid methyl esterHCID 58864518—
반응물HCID 178527016HCID 178527016—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TriethylamineHCID 8471—
생성물1-[1,4']Bipiperidinyl-1'-yl-2-(di-tert-butoxycarbonylamino)-3-(4-hydroxy-piperidin-1-yl)-propan-1-oneHCID 21102051—

반응 조건

온도0 °C

반응 단계

To a solution of 2-(di-tert-butoxycarbonylamino)-3-(4-hydroxy-piperidin-1-yl)-propionic acid methyl ester (1.0 g, 2.5 mmol) in methanol (6 mL) was added a solution of lithium hydroxide monohydrate (400 mg, 3.9 equiv) in water (1 mL). The reaction was stirred 6 h, cooled to 0° C., neutralized with concentrated hydrochloric acid, and concentrated. The crude acid was used without purification. The crude acid was suspended in methylene chloride (25 mL), treated with a few drops of methanol to aid in dissolving the acid, and cooled to 0° C. The resulting suspension was treated sequentially with 4-piperidyl-piperidine (0.53 g, 1.25 equiv), triethylamine (0.70 mL, 2. equiv), and bis-2-oxo-3-oxazolidinyl)phoshinic chloride (0.80 g, 1.25 equiv). The reaction was allowed to warm to room temperature overnight. The reaction was concentrated and then purified by Prep HPLC to afford 310 mg (23%, 2 steps). Mass spec.: 539.49 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07842808B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-c651685d1b8a46f592f6a75bb64347c5
출처 메모uspto-grants-2010_11