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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43133생성일: 2026년 10월 24일

Cesium carbonate → [5-((R)-3-hydroxy-pyrrolidin-1-ylmethyl)-pyridin-2-yl]carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/43133

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물(R)-3-PyrrolidinolHCID 2759337—
반응물tert-Butyl (5-(bromomethyl)pyridin-2-yl)carbamateHCID 23030321—
용매DimethylformamideHCID 6228—
생성물[5-((R)-3-hydroxy-pyrrolidin-1-ylmethyl)-pyridin-2-yl]carbamic acid tert-butyl esterHCID 6691459741.3%

반응 단계

A mixture of (5-methyl-pyridin-2-yl)-carbamic acid tert-butyl ester (Step 100.3) (10.7 g, 51.4 mmol), NBS (10.1 g, 56.7 mmol, 1.1 equiv), AIBN (843 mg, 5.14 mmol, 0.1 equiv) in CCl4 (500 mL) was stirred for 1 h at relfux. NBS (1.8 g, 10.1 mmol, 0.2 equiv) was added and the mixture was stirred at reflux for additional 30 min. The reaction mixture was filtered hot and the filtrate was concentrated. Trituration of the residue in CH3CN afforded of 12.88 g of impure (5-bromomethyl-pyridin-2-yl)-carbamic acid tert-butyl ester (intermediate 100.2). (R)-3-Hydroxypyrrolidine (181 mg, 2.1 mmol, 1.2 equiv) was added to a mixture of intermediate 100.2 (500 mg, 1.75 mmol) and Cs2CO3 (684 mg, 2.1 mmol, 1.2 equiv) in DMF (5 ml). The reaction mixture was stirred for 24 h at rt, quenched by addition of a saturated aqueous solution of NaHCO3 (150 mL) and extracted with EtOAc. The organic layer was washed with a saturated aqueous solution of NaHCO3, dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography (DCM/NH3aq, 99:1→DCM/MeOH/NH3aq, 96:3:1) to afford 212 mg of the title compound as a white solid. Title compound: ESI-MS: 294.3 [M+H]+; tR=1.95 min (System 1); TLC: Rf=0.14 (DCM/MeOH, 9:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536175B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-f2a83dbf186840b1b4dc2e68895fb5ed
출처 메모uspto-grants-2013_09