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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2259412생성일: 2026년 10월 27일

8-Azaspiro(4.5)decane-7,9-dione → Buspirone

https://huagongshe.com/reaction/2259412

반응식

참여 물질

역할이름HCID투입량
반응물8-Azaspiro(4.5)decane-7,9-dioneHCID 136843—
반응물8-[4-[4-(Pyrimidine-2-yl)-piperazine-1-yl]-but-2-inyl]-8-aza-spiro[4.5]decane-7,9-dioneHCID 10905038—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매ThiopheneHCID 8030—
생성물BuspironeHCID 2477100.1%

반응 단계

A solution of 100 g (0.26 mole) of 8-[4-[4-(pyrimidine-2-yl)-piperazine-1-yl]-but-2-inyl]-8-aza-spiro[4.5]decane-7,9-dione in 50 ml thiophen-free benzene is added to a suspension of 2 g of a palladium/carbon catalyst (palladium content about 5% by weight) and 50 ml of thiophen-free benzene under vigorous stirring at 20°-40° C. under the introduction of hydrogen under a pressure of 1 bar at such a rate that the hydrogen uptake of the unsaturated 8-[4-[4-pyrimidine-2-yl)-piperazine-1-yl]-but-2-inyl]-8-aza-spiro[4.5]decane-7,9-dione added is substantially identical with the calculated hydrogen consumption continuously measured with the aid of a gas burette. This practically means that when the addition of the active ingredient is stopped, the hydrogen consumption ceases within 5-10 seconds. The reaction temperature is 20°-40° C. and the reaction time is 1-4 hours. When the reduction has been terminated, the catalyst is filtered off. The catalyst can be directly used in the next hydrogenating operations without any further treatment. The filtrate is evaporated and the residue is suspended in isopropanol and filtered. Thus in the form of white crystals 100.3 g of 8-[4-[4-(pyrimidine-2yl)-piperazine-1-yl]-butyl]-8-aza-spiro[4.5]decane-7.9-dione base are obtained, yield: about 100%.Mp.:105°-106° C. (according to prior art 90°-98° C.). Content: (on the base) 99.8-100.1%. According to HPLC analysis the product contains only 0.1% of contaminations.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05473072
출처 데이터셋uspto-grants-1995_12
ORD IDord-7a45615a760f4f58ab44c9e9736f72b8
출처 메모uspto-grants-1995_12