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HRID 14754作成日:2026年10月24日

Phenylmethanesulfonyl chloride → N-{3-[(3-{2-[2-(4-Hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-methanesulfonyl-amino]-propyl}-C-phenyl-methanesulfonamide

https://huagongshe.com/ja/reaction/14754

反応式

関与物質

役割名称HCID仕込み量
反応物Phenylmethanesulfonyl chlorideHCID 74740—
反応物N-(3-Amino-propyl)-N-(3-{2-[2-(4-hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-methanesulfonamideHCID 59341031—
生成物N-{3-[(3-{2-[2-(4-Hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-methanesulfonyl-amino]-propyl}-C-phenyl-methanesulfonamideHCID 58603706—

反応手順

Compound 2 was coupled with phenyl-methanesulfonyl chloride following procedure D. LC-MS showed the product had the expected M+H+ of 610. 1H NMR (Varian 300 MHz, CD3OD, shifts relative to the solvent peak at 3.3 ppm) δ 8.3 (d, 1H), 8.0 (d, 1H) 7.5 (m, 3H) 7.3 (d, 2H), 7.2 (m, 4H), 6.7 (d, 4H), 4.4 (s, 2H), 4.2 (s, 2H), 3.6 (t, 2H), 3.2 (t, 2H), δ 2.9 (s, 3H), 2.7 (t, 2H), 2.7 (t, 2H), δ 1.6 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732444B2
出典データセットuspto-grants-2010_06
ORD IDord-b4af718ec3cb462699228b170e79463f
出典メモuspto-grants-2010_06