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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423031생성일: 2026년 10월 26일

Lithium hydroxide, monohydrate → 4-((tert-butoxycarbonylamino)methyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/423031

반응식

참여 물질

역할이름HCID투입량
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물ethyl 4-((tert-butoxycarbonylamino)methyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylateHCID 57750296—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-((tert-butoxycarbonylamino)methyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylic acidHCID 4460422163.1%

반응 조건

온도20 °C

반응 단계

Lithium hydroxide monohydrate (0.556 g, 13.26 mmol) was added to ethyl 4-((tert-butoxycarbonylamino)methyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylate (Intermediate 11) (1.07 g, 2.65 mmol) in water (6.25 ml), THF (25 ml) and ethanol (25.00 ml). The resulting solution was stirred at 20° C. for 1 day. The reaction mixture was diluted with EtOAc (20 mL) and washed with water (20 mL). The aqueous was adjusted to pH5 with 1M citric acid solution then extracted with EtOAc (3×50 mL). The organic extracts were washed with saturated brine (25 mL) then dried over MgSO4, filtered and evaporated to afford desired product 4-((tert-butoxycarbonylamino)methyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylic acid (0.628 g, 63.1%) as a white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101623B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-61da7afaeaaf4b2d9eafb3e4eca40de7
출처 메모uspto-grants-2012_01