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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1198464생성일: 2026년 10월 26일

Sodium Methoxide → 2-Butyl-5,6,7,8-tetrahydro-6-(2-hydroxy-2-methyl-1-oxopropyl)-pyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1198464

반응식

참여 물질

역할이름HCID투입량
반응물Sodium MethoxideHCID 10942334—
반응물Pentanimidamide HydrochlorideHCID 11615174—
반응물HCID 19102679HCID 19102679—
용매AcetoneHCID 180—
용매EthanolHCID 702—
용매MethanolHCID 887—
생성물2-Butyl-5,6,7,8-tetrahydro-6-(2-hydroxy-2-methyl-1-oxopropyl)-pyrido[4,3-d]pyrimidin-4(3H)-oneHCID 13567496981.4%

반응 단계

A mixture of 0.7 g of ethyl 1-(2-hydroxy-2-methyl-1-oxopropyl)-4-oxo-3-piperidinecarboxylate and 0.4 g of valeramidine hydrochloride in 8 ml of anhydrous ethyl alcohol is treated with 2.8 ml of a 1M solution of sodium methoxide in methanol. The resulting mixture is stirred and heated at reflux for one hour. The reaction mixture is allowed to cool over 30 minutes then filtered. The filtrate is evaporated to a syrup which is stirred with 50 ml of ether overnight. The ether is decanted to afford a oily solid which is dissolved in acetone and applied to thick layer silica gel plates. The plates are eluted with ethyl acetate and the major zone washed stirred with water and the water decanted. The residue is dried and chromatographed on thick layer silica gel chromatography plates using ethyl acetate as the elution solvent. The major band at Rf=0.2 is isolated by washing with acetone to afford 0.65 g of the desired product as a colorless solid, m.p. 159°-161° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05281602
출처 데이터셋uspto-grants-1994_01
ORD IDord-1fe5d88bb3154b16b4e530621125448c
출처 메모uspto-grants-1994_01