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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Methoxy-N-methylbenzamide | HCID 569575 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | 6-Methyl-4-(methylthio)thieno[3,2-d]pyrimidine | HCID 17965831 | — |
| 반응물 | 2-[4-(Methylthio)thieno[3,2-d]pyrimidin-6-yl]-1-phenylethanone | HCID 17965867 | — |
| 반응물 | Sodium Nitrite | HCID 23668193 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-[4-(Methylthio)thieno[3,2-d]pyrimidin-6-yl]-2-phenylethane-1,2-dione 1-oxime | HCID 136337744 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07427616B2 |
|---|
| 출처 데이터셋 | uspto-grants-2008_09 |
|---|
| ORD ID | ord-997f413299d9486e842b4c251643a252 |
|---|
| 출처 메모 | uspto-grants-2008_09 |
|---|