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HRID 390864作成日:2026年10月26日

5-(Tributylstannyl)-1,3-thiazole → 4-morpholino-6-((4-N-methylsulfonylpiperazin-1-yl)methyl)-2-(thiazol-5-yl)thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/390864

反応式

関与物質

役割名称HCID仕込み量
反応物5-(Tributylstannyl)-1,3-thiazoleHCID 2763257—
反応物4-(2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholineHCID 23650837—
触媒HCID 178418397HCID 178418397—
溶媒DimethylacetamideHCID 31374—
生成物4-morpholino-6-((4-N-methylsulfonylpiperazin-1-yl)methyl)-2-(thiazol-5-yl)thieno[3,2-d]pyrimidineHCID 5823404450%

反応条件

温度150 °C

反応手順

A suspension of 2-chloro-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine, prepared via General Procedure B-3, (144 mg, 0.33 mmol), 5-tributylstannanyl-thiazole (187 mg, 0.5 mmol), and Pd(PPh3)4 (19 mg, 0.017 mmol) in anhydrous DMA was heated in a microwave at 150° C. for 10 mins. The crude reaction was loaded onto a preconditioned SCX cartridge, washing the cartridge with methanol and dichloromethane before eluting with 7N ammonia in methanol to give crude material. This was purified by on silica using 5% methanol in ethyl acetate as the eluent to give 152 as an off-white solid (80 mg, 50%). NMR (CDCl3, 400 MHz), 2.68-2.72 (4H, m), 2.83 (3H, s), 3.32-3.36 (4H, m), 3.88-3.93 (6H, m), 4.03-4.06 (4H, m), 7.32 (1H, s), 8.67 (1H, m), 8.84 (1H, s). MS: (ESI+): MH+=481

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383620B2
出典データセットuspto-grants-2013_02
ORD IDord-0e0f3e8f7b7146c692ea2f769a0a9710
出典メモuspto-grants-2013_02