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【结 构 式】

【药物名称】N-2733

【化学名称】1-[3-(3-Pyridinyl)-2(E)-propenoyl]-2-pyrrolidinone hydrochloride

【CA登记号】141236-60-4 (free base), 132220-88-3 (undefined isomer;free base)

【 分 子 式 】C12H13ClN2O2

【 分 子 量 】252.70261

【开发单位】Nisshin Pharma (Originator)

【药理作用】ANTIINFECTIVE THERAPY, Treatment of Septic Shock, Antiinflammatory Drugs, TNF-alpha Production Inhibitors

合成路线1

Treatment of 3-(3-pyridyl)acrylic acid (I) with oxalyl chloride afforded the corresponding acid chloride (II). This was coupled with 1-trimethylsilyl-2-pyrrolidinone (IV) (prepared from pyrrolidinone (III) and hexamethyldisilazane), to produce the target imide.

1 Nagasaka, T.; et al.; Synthesis of 1-trans-cinnamoyl- and 1-[trans-3-(pyridyl)acryloyl]-2-pyrrolidinone derivatives and their effect on hemicholinium-induced impairment of water maze learning in mice. Yakugaku Zasshi 1992, 112, 2, 100.
2 Nagasaka, T.; Yamada, H.; Hamaguchi, F. (Nisshin Flour Milling Co., Ltd.); Pyrrolidinone derivs.. JP 1990225458 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 29291 (E)-3-(3-pyridinyl)-2-propenoic acid 19337-97-4 C8H7NO2 详情 详情
(II) 29292 (E)-3-(3-pyridinyl)-2-propenoyl chloride C8H6ClNO 详情 详情
(III) 27397 2-Pyrrolidinone 616-45-5 C4H7NO 详情 详情
(IV) 29293 1-(trimethylsilyl)-2-pyrrolidinone 14468-90-7 C7H15NOSi 详情 详情
Extended Information