돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 639088생성일: 2026년 10월 26일

(+/-)-Phenylmethyl[(trans-1-{2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]ethyl}-4-hydroxy-3-pyrrolidinyl)methyl]carbamate → (+/-)-Trans-4-(aminomethyl)-1-{2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]ethyl}-3-pyrrolidinol

https://huagongshe.com/reaction/639088

반응식

참여 물질

역할이름HCID투입량
반응물(+/-)-Phenylmethyl[(trans-1-{2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]ethyl}-4-hydroxy-3-pyrrolidinyl)methyl]carbamateHCID 131728028—
촉매Palladium hydroxideHCID 9942167—
용매MethanolHCID 887—
생성물(+/-)-Trans-4-(aminomethyl)-1-{2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]ethyl}-3-pyrrolidinolHCID 68818112102.5%

반응 단계

To a solution of (±)-phenylmethyl[(trans-1-{2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]ethyl}-4-hydroxy-3-pyrrolidinyl)methyl]carbamate (1.8 g, 3.96 mmole) in MeOH (100 mL) in a round bottom flask was added Pd(OH)2 (˜100 mg). The reaction contents were stirred under a balloon of H2 overnight at RT. The reaction contents were filtered through Celite® (MeOH) and concentrated to give the title compound (1.3 g, quant.) as a light yellow foam: LC-MS (ES) m/e 321 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691850B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-4bcac6bc834b497382065093040d247f
출처 메모uspto-grants-2010_04