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【结 构 式】

【分子编号】59847

【品名】2,3-dihydro-1-benzofuran-5-sulfonic acid

【CA登记号】

【 分 子 式 】C8H8O4S

【 分 子 量 】200.21512

【元素组成】C 47.99% H 4.03% O 31.96% S 16.02%

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)

Electrophilic sulfonation of 2,3-dihydrobenzofuran (I) using sulfur trioxide-dimethylformamide complex produced sulfonic acid (II), which was subsequently converted into the sulfonyl chloride (III) by chlorination with SOCl2. Reaction of sulfonyl chloride (III) with a solution of ammonia in cold dichloroethane gave rise to the sulfonamide (IV). This was subsequently condensed with 3,4-dichlophenyl isocyanate (V) to furnish the target sulfonyl urea

1 Tao, E.V.-P.; Miller, W.D. (Eli Lilly and Company); Synthesis of bicyclic aromatic sulfonic acids, sulfonyl chlorides and sulfonamides. EP 0583960 .
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) 14499 2,3-Dihydrobenzofuran; 2,3-dihydro-1-benzofuran 496-16-2 C8H8O 详情 详情
(II) 59847 2,3-dihydro-1-benzofuran-5-sulfonic acid C8H8O4S 详情 详情
(III) 59848 2,3-dihydro-1-benzofuran-5-sulfonyl chloride C8H7ClO3S 详情 详情
(IV) 59849 2,3-dihydro-1-benzofuran-5-sulfonamide C8H9NO3S 详情 详情
(V) 34282 1,2-dichloro-4-isocyanatobenzene; 3,4-dichlorophenyl isocyanate 102-36-3 C7H3Cl2NO 详情 详情
Extended Information