Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379569생성일: 2026년 10월 26일
1-methyl-1H-1,3-benzodiazole-2-carbaldehyde → (+/-)-6-[1-Hydroxy-1-(1-methyl-1H-benzimidazol-2-yl)methyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/379569
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-methyl-1H-1,3-benzodiazole-2-carbaldehyde | HCID 762084 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 3-Methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione | HCID 5282527 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (+/-)-6-[1-Hydroxy-1-(1-methyl-1H-benzimidazol-2-yl)methyl]-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione | HCID 9930755 | 15.5% |
반응 단계
A solution of lithium diisopropylamide (3.15 mmol) in anhydrous tetrahydrofuran (5 ml) was added to a solution of 3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (500 mg) in anhydrous tetrahydrofuran (20 ml) at −78° C. After 10 minutes, 1-methylbenzimidazole-2-carboxaldehyde (600 mg) was added and the resultant solution kept at −78° C. for 1 hour. The reaction mixture was allowed to warm to ambient temperature and quenched with saturated sodium hydrogen carbonate solution. The mixture was extracted with ethyl acetate and washed with saturated sodium hydrogen carbonate and then brine, then dried over a mixture of magnesium sulfate and silica, filtered, and evaporated. Purification by HPLC over silica eluting with an isohexane:ethyl acetate gradient (4:1 to 0:1) gave the title compound (0.13 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06300334B1 |
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| 출처 데이터셋 | uspto-grants-2001_10 |
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| ORD ID | ord-a42dadee039c4c8cab9e92fadd8430e2 |
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| 출처 메모 | uspto-grants-2001_10 |
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