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【结 构 式】

【分子编号】37130

【品名】methyl trimethoxymethyl ether; tetramethoxymethane

【CA登记号】1850-14-2

【 分 子 式 】C5H12O4

【 分 子 量 】136.14788

【元素组成】C 44.11% H 8.88% O 47.01%

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:(II)

The reaction of 5-amino-4-cyanooxazole (I) with tetramethyl orthocarbonate (II) in refluxing acetic anhydride gives 4-cyano-5-(diethoxymethyleneamino)oxazole (III), which is cyclized with propylamine (A) in refluxing ethanol yielding 5-methoxy-6-propyl-7(6H)-iminooxazolo[5,4-d]pyrimidine (IV), which is finally hydrolyzed and rearranged by treatment with NaOH in water at 100 C or with formamide at 180 C.

1 Ohtsuka, Y.; Oxazolopyrimidines. VI. Formation of 3-substituted xanthines via 7-(6H)-iminooxazolopyrimidines. Bull Chem Soc Jpn 1973, 46, 2, 506-509.
2 Sneddon, J.M.; Castaner, J.; Blancafort, P.; Serradell, M.N.; Enprofylline. Drugs Fut 1982, 7, 9, 623.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(A) 23923 1-propanamine 107-10-8 C3H9N 详情 详情
(I) 37129 5-amino-1,3-oxazole-4-carbonitrile C4H3N3O 详情 详情
(II) 37130 methyl trimethoxymethyl ether; tetramethoxymethane 1850-14-2 C5H12O4 详情 详情
(III) 37131 4-cyano-5-[(dimethoxymethylene)amino]-1,3-oxazole C7H7N3O3 详情 详情
(IV) 37132 5-methoxy-6-propyl[1,3]oxazolo[5,4-d]pyrimidin-7(6H)-imine C9H12N4O2 详情 详情
Extended Information