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HRID 1365403作成日:2026年10月25日

2,3-Dimethylpyridine-5-boronic acid pinacol ester → 4-(2-(5,6-Dimethylpyridin-3-yl)-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)thieno[2,3-d]pyrimidin-4-yl)morpholine

https://huagongshe.com/reaction/1365403

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dimethylpyridine-5-boronic acid pinacol esterHCID 53216810—
反応物2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinothieno[2,3-d]pyrimidineHCID 56833946—
生成物4-(2-(5,6-Dimethylpyridin-3-yl)-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)thieno[2,3-d]pyrimidin-4-yl)morpholineHCID 24947052—

反応手順

2,3-Dimethyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine was reacted with 2-chloro-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[2,3-d]pyrimidine in General Procedure A. Purification on silica yielded 371. NMR: (CDCl3): (400 MHz, CDCl3): 2.40 (3H, s, Me), 2.59 (3H, s, Me), 2.63-2.68 (4H, m), 2.82 (3H, s, Me), 3.29-3.31 (4H, m), 3.84 (2H, s, CH2), 3.90-3.92 (4H, m), 3.98-4.00 (4H, m), 7.17 (1H, s, Ar), 8.41 (1H, s, Ar) and 9.35 (1H, s, Ar). MS: (ESI+): MH+503.15

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07888352B2
出典データセットuspto-grants-2011_02
ORD IDord-77ca6b09221c47048c440b9b3f79a7e2
出典メモuspto-grants-2011_02