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HRID 567917作成日:2026年10月26日

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/567917

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-CyanobenzaldehydeHCID 101209—
反応物Lithium diisopropylamideHCID 2724682—
反応物3-Methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 5282527—
溶媒TetrahydrofuranHCID 8028—
生成物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)-dioneHCID 22258043—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06180635B2
出典データセットuspto-grants-2001_01
ORD IDord-998a81851c3e4775950226110ecde8a5
出典メモuspto-grants-2001_01