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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1611040생성일: 2026년 10월 26일

Water → 6-(3-Imino-1,3-dihydro-benzo[c]furan-1-yl)-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1611040

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-CyanobenzaldehydeHCID 101209—
반응물Lithium diisopropylamideHCID 2724682—
반응물3-Methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 5282527—
용매TetrahydrofuranHCID 8028—
생성물6-(3-Imino-1,3-dihydro-benzo[c]furan-1-yl)-3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 22258043—

반응 단계

To a solution of 3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidin-2,4(1H,3H)-dione (500 mg) in tetrahydrofuran (10 ml) at −78° C. was added lithium diisopropylamide (1M, 3.1 ml). After 5 minutes a solution of o-cyanobenzaldehyde in tetrahydrofuran (2 ml) was added and the reaction was allowed to stir for 2 h. Water (10 ml) was the added and the mixture was allowed to warm to room temperature. The mixture was extracted with ethyl acetate. The organic layer was separated and dried over magnesium sulfate, then concentrated in vacuo and purified by normal phase HPLC to yield the title compound (15 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06984644B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-aff7b997f2664c789928d1ee50102143
출처 메모uspto-grants-2006_01