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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362098생성일: 2026년 10월 24일

tert-Butyl acrylate → (E)-3-(6-Amino-5-piperidin-1-ylmethyl-pyridin-3-yl)acrylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/1362098

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl acrylateHCID 15458—
반응물Tri-o-tolylphosphineHCID 80271—
반응물DiisopropylethylamineHCID 81531—
반응물5-Bromo-3-piperidin-1-ylmethyl-pyridin-2-ylamineHCID 59456983—
촉매palladium(II) acetateHCID 167845—
용매PropionitrileHCID 7854—
생성물(E)-3-(6-Amino-5-piperidin-1-ylmethyl-pyridin-3-yl)acrylic acid tert-butyl esterHCID 5945693160%

반응 단계

A solution of 5-bromo-3-piperidin-1-ylmethyl-pyridin-2-ylamine (500 mg, 1.85 mmol), tert-butyl acrylate (0.3 mL, 2.0 mmol), (i-Pr)2EtN (0.5 mL, 2.8 mmol) and P(o-tol)3 (114 mg, 0.37 mmol) in EtCN (10 mL) was de-oxygenated with argon for 30 min. Pd(OAc)2 (43 mg, 0.19 mmol) was added, and the mixture was de-oxygenated for 15 min. The mixture was heated to reflux for 18 h and then allowed to cool. The solvent was removed in vacuo. The residue was partitioned between EtOAc and H2O. The organic layer was washed with H2O and satd NaCl, dried over Na2SO4 and concentrated. Purification by column chromatography (silica gel, CH2Cl2 to 96:4 CH2Cl2/CH3OH) gave the title compound (350 mg, 60%) as a yellow solid: MS (ESI) m/e 318 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-5ba8fdefc565475a8d58ef676427d959
출처 메모uspto-grants-2011_02