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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 137생성일: 2026년 10월 24일

3-Aminoazetidine, 3-BOC protected → tert-butyl N-[1-(2-methoxy-4-pyridinyl)azetidin-3-yl]carbamate

https://huagongshe.com/ko/reaction/137

반응식

참여 물질

역할이름HCID투입량
반응물3-Aminoazetidine, 3-BOC protectedHCID 1519405—
반응물4-Bromo-2-methoxypyridineHCID 14062309—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물tert-butyl N-[1-(2-methoxy-4-pyridinyl)azetidin-3-yl]carbamateHCID 11805502999.96%

반응 조건

온도70 °C

반응 단계

A mixture of all the reactants in toluene was heated in a sealed vial at 70 °C overnight. According to LC-MS the reaction was completed and the product had been formed. Toluene was removed, water was added and the product was extracted with DCM. The organic phase was dried through phase separator and concentrated.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-f3ebf4dfde174cff92751e3b49ce74da
출처 메모750 AstraZeneca ELN dataset