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【结 构 式】

【分子编号】27888

【品名】4-(1,3-dioxolan-2-yl)-2-pyridinyl (Z)-4-(tetrahydro-2H-pyran-2-yloxy)-2-butenyl ether

【CA登记号】

【 分 子 式 】C17H23NO5

【 分 子 量 】321.37336

【元素组成】C 63.54% H 7.21% N 4.36% O 24.89%

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:(III)

A new synthesis of lafutidine has been described: The condensation of 2-bromopyridine-4-carbaldehyde ethylene ketal (I) with 4-(tetrahydropyranyloxy)-2(Z)-buten-1-ol (II) by means of NaOH, K2CO3 and tetrabutylammonium bisulfate in refluxing toluene gives the corresponding substitution product (III), which by treatment with pyridinium p-toluenesulfonate (PPTS) in hot ethanol yields the 2(Z)-butenol (IV). The reaction of (IV) with SOCl2 and then with potassium phthalimide (V) affords the substituted phthalimide (VI), which by treatment with hydrazine hydrate in refluxing methanol gives the 2(Z)-butenamine (VII). The condensation of (VII) with 2-(2-furylmethylsulfinyl)acetic acid 4-nitrophenyl ester (VIII) in THF yields the expected amide (IX), which is treated with p-toluenesulfonic acid in refluxing acetone/water to eliminate the ethylene ketal protecting group yilding the aldehyde (X). Finally, this compound is reductocondensed with piperidine (XI) by means of NaBH4 in ethanol.

1 Hosoda, A.; Yamaura, T.; Sekine, Y.; Matsumoto, H.; Hirakawa, N.; Sekine, A.; A novel histamine 2(H2) receptor antagonist with gastroprotective activity. II. Synthesis and pharmacological evaluation of 2-furfuryl-thio and 2-furfurylsulfinyl acetamide derivatives with heteroaromatic rings. Chem Pharm Bull 1998, 46, 4, 616.
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) 27887 2-bromo-4-(1,3-dioxolan-2-yl)pyridine C8H8BrNO2 详情 详情
(II) 13026 (Z)-4-(Tetrahydro-2H-pyran-2-yloxy)-2-buten-1-ol C9H16O3 详情 详情
(III) 27888 4-(1,3-dioxolan-2-yl)-2-pyridinyl (Z)-4-(tetrahydro-2H-pyran-2-yloxy)-2-butenyl ether C17H23NO5 详情 详情
(IV) 27889 (Z)-4-[[4-(1,3-dioxolan-2-yl)-2-pyridinyl]oxy]-2-buten-1-ol C12H15NO4 详情 详情
(V) 27890 Potassium phthalimide 1074-82-4 C8H4KNO2 详情 详情
(VI) 27891 2-((Z)-4-[[4-(1,3-dioxolan-2-yl)-2-pyridinyl]oxy]-2-butenyl)-1H-isoindole-1,3(2H)-dione C20H18N2O5 详情 详情
(VII) 27892 (Z)-4-[[4-(1,3-dioxolan-2-yl)-2-pyridinyl]oxy]-2-butenylamine C12H16N2O3 详情 详情
(VIII) 13031 4-nitrophenyl 2-[(2-furylmethyl)sulfinyl]acetate C13H11NO6S 详情 详情
(IX) 27893 N-((Z)-4-[[4-(1,3-dioxolan-2-yl)-2-pyridinyl]oxy]-2-butenyl)-2-[(2-furylmethyl)sulfinyl]acetamide C19H22N2O6S 详情 详情
(X) 27894 N-[(Z)-4-[(4-formyl-2-pyridinyl)oxy]-2-butenyl]-2-[(2-furylmethyl)sulfinyl]acetamide C17H18N2O5S 详情 详情
(XI) 10158 Piperidine 110-89-4 C5H11N 详情 详情
Extended Information