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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62214생성일: 2026년 10월 26일

tert-butyl (3S)-3-aminopiperidine-1-carboxylate → (3S)-tert-butyl 3-(4-(5-(3,4-dimethoxyphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl)picolinamido)piperidine-1-carboxylate

https://huagongshe.com/reaction/62214

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
반응물4-(5-(3,4-Dimethoxyphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl)picolinic acidHCID 136344397—
생성물(3S)-tert-butyl 3-(4-(5-(3,4-dimethoxyphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl)picolinamido)piperidine-1-carboxylateHCID 13634439843%

반응 단계

Example ER-897036 was prepared in two steps from 4-(5-(3,4-dimethoxyphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl)picolinic acid (25 mg, 0.056 mmol) and commercially available (S)-tert-butyl 3-aminopiperidine-1-carboxylate (33 mg, 0.167 mmol) in a manner similar to that of example D-6 to afford intermediate (3S)-tert-butyl 3-(4-(5-(3,4-dimethoxyphenyl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-2-yl)picolinamido)piperidine-1-carboxylate (15 mg, 0.024 mmol, 43% yield). Then, this intermediate (13 mg, 0.021 mmol) was treated with HCl in a manner similar to that of example ER-897560 to afford the desired product ER-897036 (12 mg, 96% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09446046B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-a7d8eb7167004028aa1fc1ee7ab4aad5
출처 메모uspto-grants-2016_09