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【结 构 式】

【药物名称】CI-844

【化学名称】3-Phenoxypyridine sulfate

【CA登记号】2176-45-6 (free base), 66066-82-8 (HBr salt), 66066-81-7 (HCl), 66066-84-0 (methanesulfonate)

【 分 子 式 】C11H11NO5S

【 分 子 量 】269.27802

【开发单位】Pfizer (Originator)

【药理作用】Cognition Disorders, Treatment of, NEUROLOGIC DRUGS

合成路线1

3-Phenoxypyridine can be prepared by two different ways: 1) By reaction of 3-hydroxypyridine (I) with bromobenzene (II) by means of KOH and copper bronze at 150 C. 2) By reaction of 3-iodopyridine (III) with phenol (IV) by means of KOH and copper bronze at 150 C. The monosulfate salt is prepared by treating 3-phenoxypyridine with H2SO4.

1 Renshaw, R.R.; Conn, R.C.; Quaternary deivation of pyridyl ethers. Onium Compound. XVI. J Am Chem Soc 1937, 59, 297-301.
2 Butler, D.E. (Pfizer Inc.); 3-Phenoxypyridine monosulfate and a method for its production. BE 0861649; DE 2755016; ES 464922; FR 2392009; GB 1559918; JP 53077068; US 4128555 .
3 Owen, R.T.; Castaner, J.; Serradell, M.N.; CI-844. Drugs Fut 1985, 10, 4, 279.
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) 13365 Monobromobenzene; 1-Bromobenzene;Phenylbromide;bromobenzene 108-86-1 C6H5Br 详情 详情
(II) 12911 3-Hydroxypyridine; 3-Pyridinol 109-00-2 C5H5NO 详情 详情
(III) 29108 3-iodopyridine C5H4IN 详情 详情
(IV) 23540 Phenol 108-95-2 C6H6O 详情 详情
Extended Information