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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1458603생성일: 2026년 10월 26일

N-[(1-benzyl-4-piperidyl)methyl] 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamide oxalate salt → N-(4-Piperidylmethyl) 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamide

https://huagongshe.com/reaction/1458603

반응식

참여 물질

역할이름HCID투입량
반응물N-[(1-benzyl-4-piperidyl)methyl] 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamide oxalate saltHCID 19599416—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
생성물N-(4-Piperidylmethyl) 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamideHCID 9839803105.4%

반응 단계

A stirred suspension of N-[(1-benzyl-4-piperidyl)methyl] 3,4-dihydro-2 H-[1,3]oxazino[3,2-a]indole-10-carboxamide oxalate salt (E20, 2.25 g, 0.0046 mole) in ethanol (100 ml) and glacial acetic acid (4 ml) was hydrogenated over 10% Pd--C (0.8 g) at atmospheric pressure and 45° C. for 18 h. The mixture was filtered and the filtrate concentrated in vacuo. The majority of the product was in the solid which had been filtered off. This material was shaken with concentrated potassium carbonate solution (50 ml) and chloroform (50 ml) together with the residue from the filtrate. The mixture was filtered, the chloroform layer separated and dried (Na2SO4), then concentrated in vacuo to afford the title compound as a white solid (1.52 g, 100%). This was recrystallised from chloroform/60-80 petrol mp 139°-141° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05852014
출처 데이터셋uspto-grants-1998_12
ORD IDord-eea20efdfad441b6aefc67659877da3c
출처 메모uspto-grants-1998_12