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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32533생성일: 2026년 10월 24일

N-Methoxy-N-methylbenzamide → 1-[4-(Methylthio)thieno[3,2-d]pyrimidin-6-yl]-2-phenylethane-1,2-dione 1-oxime

https://huagongshe.com/ko/reaction/32533

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참여 물질

역할이름HCID투입량
반응물N-Methoxy-N-methylbenzamideHCID 569575—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물6-Methyl-4-(methylthio)thieno[3,2-d]pyrimidineHCID 17965831—
반응물2-[4-(Methylthio)thieno[3,2-d]pyrimidin-6-yl]-1-phenylethanoneHCID 17965867—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-[4-(Methylthio)thieno[3,2-d]pyrimidin-6-yl]-2-phenylethane-1,2-dione 1-oximeHCID 13633774486%

반응 조건

온도0 °C

반응 단계

6-Methyl-4-(methylthio)thieno[3,2-d]pyrimidine, (intermediate 22) (665 mg) was dissolved in THF (10 mL) and added slowly, over 15 minutes, to a stirred solution of LHMDS in THF (1M, 3.39 mL) at −78° C. After 10 minutes, N-methoxy-N-methylbenzamide (616 mg) was added and the reaction mixture warmed to 0° C. After 2 hours at 0° C. the resultant solution of 2-[4-(methylthio)thieno[3,2-d]pyrimidin-6-yl]-1-phenylethanone was acidified with acetic acid (10 mL), diluted with water (10 mL) and re-cooled to 0° C. Sodium nitrite (280 mg) was added and the mixture was stirred overnight. After evaporation of the solvents, the solid residue was collected with water by filtration, and dried to give the title compound as a brown solid (959 mg, 86%);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427616B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-997f413299d9486e842b4c251643a252
출처 메모uspto-grants-2008_09