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【结 构 式】

【分子编号】45190

【品名】potassium 1-(carbodithioatooxy)ethane

【CA登记号】

【 分 子 式 】C3H5KOS2

【 分 子 量 】160.3024

【元素组成】C 22.48% H 3.14% K 24.39% O 9.98% S 40.01%

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:(I)

A new synthesis of [14C]-labeled pantoprazole has been described: The cyclization of potassium [14C]-ethylxanthate (I) with the diaminobenzene (II) by means of NaOH gives the imidazole (III), which is condensed with 2-(chloromethyl)-3,4-dimethoxypyridine (IV) by means of NaOH in ethanol to afford the sulfide (V). Finally, this compound is oxidized with m-chloroperbenzoic acid (mcpba) in dichloromethane.

1 Saunders, D.; Lawrie, K.W.M.; Crowe, A.M.; Johnston, C.E.A.; The synthesis of [14C]pantoprazole - SK&F 96022Z - An H+/K+ ATP inhibitor. J Label Compd Radiopharm 1992, 31, 5, 409.
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) 14032 Dithiocarbonic acid O-ethyl ester potassium salt C3H5KOS2 详情 详情
(I) 45190 potassium 1-(carbodithioatooxy)ethane C3H5KOS2 详情 详情
(II) 14033 4-(Difluoromethoxy)-1,2-benzenediamine; 2-Amino-4-(difluoromethoxy)phenylamine C7H8F2N2O 详情 详情
(III) 14034 5-(Difluoromethoxy)-1H-benzimidazole-2-thiol; 5-(Difluoromethoxy)-1H-benzimidazol-2-ylhydrosulfide; 5-Difluoromethoxy-2-mercapto-1H-benzimidazole 97963-62-7 C8H6F2N2OS 详情 详情
(III) 45191 5-(difluoromethoxy)-1H-benzimidazole-2-thiol; 5-(difluoromethoxy)-1H-benzimidazol-2-ylhydrosulfide C8H6F2N2OS 详情 详情
(IV) 14035 2-(Chloromethyl)-3,4-dimethoxypyridine; 2-(Chloromethyl)-3-methoxy-4-pyridinyl methyl ether 72830-09-2 C8H10ClNO2 详情 详情
(V) 14036 5-(Difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridinyl)methyl]sulfanyl]-1H-benzimidazole; 2-([[5-(Difluoromethoxy)-1H-benzimidazol-2-yl]sulfanyl]methyl)-3-methoxy-4-pyridinyl methyl ether 102625-64-9 C16H15F2N3O3S 详情 详情
(V) 45192 2-([[5-(difluoromethoxy)-1H-benzimidazol-2-yl]sulfanyl]methyl)-3-methoxy-4-pyridinyl methyl ether; 5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridinyl)methyl]sulfanyl]-1H-benzimidazole C16H15F2N3O3S 详情 详情
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