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【结 构 式】

【药物名称】

【化学名称】1-(3,4-Dichlorobenzyl)-3,4-dihydro-1H-2,1,3-benzothiadiazin-4-one S,S-dioxide

【CA登记号】

【 分 子 式 】C14H10Cl2N2O3S

【 分 子 量 】357.2174

【开发单位】Almirall Prodesfarma (Originator), CSIC (Originator)

【药理作用】PHARMACOLOGICAL TOOLS, Phosphodiesterase Inhibitors

合成路线1

Benzothiadiazine S,S-dioxide (II) was obtained by a two-step condensation of methyl anthranylate (I) and sulfamoyl chloride following a reported procedure (1). The alkylation of (II) with 3,4-dichlorobenzyl chloride (III) in the presence of NaHCO3 furnished the title compound.

1 J Am Chem Soc 1962, 84, 1994-2000.
2 Castro, A.; Gil, C.; Martinez, A.; et al.; Benzyl derivatives of 2,1,3-benzo- and benzothieno[3,2-a]thiadiazine 2,2-dioxides: First phosphodiesterase 7 inhibitors. J Med Chem 2000, 43, 4, 683.
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) 11161 methyl 2-aminobenzoate; Methyl anthranilate 134-20-3 C8H9NO2 详情 详情
(II) 34452 2lambda(6),1,3-benzothiadiazine-2,2,4(1H,3H)-trione C7H6N2O3S 详情 详情
(III) 19333 1,2-dichloro-4-(chloromethyl)benzene 102-47-6 C7H5Cl3 详情 详情
Extended Information