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HRID 881445作成日:2026年10月27日

Methanesulfonylmethanesulfonyl chloride → 2-Chloro-6-(4-methanesulfonylmethanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/881445

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonylmethanesulfonyl chlorideHCID 556269—
反応物4-(2-Chloro-6-(piperazin-1-ylmethyl)thieno[3,2-d]pyrimidin-4-yl)morpholineHCID 57494057—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物2-Chloro-6-(4-methanesulfonylmethanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidineHCID 87209439—

反応手順

To 2-chloro-4-morpholino-6-((piperazin-1-yl)methyl)thieno[3,2-d]pyrimidine (54 mg) in DCM (2 ml) and triethylamine (44 ul) was added methylsulfonylmethylsulfonyl chloride (45 ul) at 0° C. The reaction mixture was allowed to warm up to room temperature overnight. Aqueous work-up and purification on silica gave 2-chloro-6-(4-methanesulfonylmethanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (35 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993563B2
出典データセットuspto-grants-2015_03
ORD IDord-12721725d88f49158af0687a9d3f9550
出典メモuspto-grants-2015_03