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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 911생성일: 2026년 10월 23일

Risperidone → 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one 4,4'-methylenebis[3-hydroxy-2-naphthalenecarboxylate]

https://huagongshe.com/ko/reaction/911

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참여 물질

역할이름HCID투입량
반응물RisperidoneHCID 5073—
반응물Pamoic AcidHCID 8546—
용매EthanolHCID 702—
용매DimethylformamideHCID 6228—
생성물3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one 4,4'-methylenebis[3-hydroxy-2-naphthalenecarboxylate]HCID 983224881%

반응 단계

A solution of 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (0.048mol) in ethanol (600ml) was added to a solution of pamoic acid (0.048mol) in N,N-dimethylformamide (400ml). The mixture was stirred for 3 hours. The resulting precipitate was filtered off by suction, washed with ethanol and dried, yielding 31 g (81%) of 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one 4,4'-methylenebis[3-hydroxy-2-naphthalenecarboxylate](1:1); mp. 269.2° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723467
출처 데이터셋uspto-grants-1998_03
ORD IDord-2a631a89ec7e4caea3676f4cb6dcf4c2
출처 메모uspto-grants-1998_03