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HRID 41894作成日:2026年10月25日

Trimethyl orthoformate → 4-(2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholine

https://huagongshe.com/reaction/41894

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl orthoformateHCID 9005—
反応物1-(Methylsulfonyl)piperazineHCID 709161—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-Chloro-4-morpholinothieno[3,2-d]pyrimidine-6-carbaldehydeHCID 45789985—
溶媒1,2-DichloroethaneHCID 11—
生成物4-(2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholineHCID 2365083766.3%

反応手順

A mixture of 2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidine-6-carbaldehyde 10 (1.00 g), 1-methanesulfonyl-piperazine (750 mg) and trimethylorthoformate (3.80 mL) was stirred in 1,2-dichloroethane (30 mL) for 6 hrs at room temperature. To this was added sodium triacetoxyborohydride (900 mg) and the reaction mixture was stirred for 24 hours at room temperature. The mixture was then quenched with brine, extracted with dichloromethane, dried (MgSO4) and the solvent removed in vacuo. The residue was triturated with hot ethyl acetate to yield 4-(2-chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholine 31 as a white solid (1.01 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536161B2
出典データセットuspto-grants-2013_09
ORD IDord-faa11640f68b4d978d0f84d532464ca4
出典メモuspto-grants-2013_09