돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물1-methyl-1H-1,3-benzodiazole-2-carbaldehydeHCID 762084—
반응물Lithium diisopropylamideHCID 2724682—
반응물3-Methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 5282527—
용매TetrahydrofuranHCID 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)-dioneHCID 993075515.5%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300334B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-a42dadee039c4c8cab9e92fadd8430e2
출처 메모uspto-grants-2001_10