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【结 构 式】

【分子编号】13338

【品名】2-Methyl-1-(1-piperidinyl)-2-propanol

【CA登记号】

【 分 子 式 】C9H19NO

【 分 子 量 】157.256

【元素组成】C 68.74% H 12.18% N 8.91% O 10.17%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(IV)

The chlorination of 2-phenyl-3-methyl-4-oxo-4H-1-benzopyran-8-carboxylic acid (I) with thionyl chloride gives the corresponding chloride (II), which is esterified with 1,1-dimethyl-2-(1-piperidinyl)ethanol (IV), obtained by alkylation of excess piperidine (III) with 1-chloro-2-methyl-2-propanol. Rec 15/2053 is obtained as the hydrochloride.

1 Williams, M.E.; Pannil, C.; Urinary incontinence in the elderly. Physiology, pathophysiology, diagnosis and treatment. Ann Intern Med 1982, 97, 6, 895-907.
2 Nardi, D.; Tajana, A.; Cazzulati, P.; Graziani, G.; Pennini, R.; Casadio, S. (Recordati Industria Chimica e Farmaceutica SpA); 3-Methylflavone-8-carboxylic acid esters. EP 0072620; GB 2104507 .
3 Testa, R.; Leonardi, A.; Tajana, A.; Terflavoxate Hydrochloride. Drugs Fut 1994, 19, 3, 248.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
24160 1-chloro-2-methyl-2-propanol 558-42-9 C4H9ClO 详情 详情
(I) 13335 3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic acid; 3-Methylflavone-8-carboxylic acid 3468-01-7 C17H12O4 详情 详情
(II) 13336 3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carbonyl chloride C17H11ClO3 详情 详情
(III) 10158 Piperidine 110-89-4 C5H11N 详情 详情
(IV) 13338 2-Methyl-1-(1-piperidinyl)-2-propanol C9H19NO 详情 详情
Extended Information