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【结 构 式】

【分子编号】27727

【品名】N-(2-iodophenyl)-6-methoxy-3,4-dihydro-1-naphthalenecarboxamide

【CA登记号】

【 分 子 式 】C18H16INO2

【 分 子 量 】405.23505

【元素组成】C 53.35% H 3.98% I 31.32% N 3.46% O 7.9%

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)

Condensation of of 2-iodoaniline (I) with vinyl triflate (II) in the presence of Pd(PPh3)4 and K2CO3 under atmosphere of CO produced the intermediate amide, which underwent an annellation reaction to the title benzoxazinone.

1 Arcadi, A.; et al.; Synthesis and in vitro and in vivo evaluation of the 2-(6'methoxy-3',4'-dihydro-1'-naphtyl)-4H-3,1-benzoxazin-4-one as a new potent substrate inhibitor of human leukocyte elastase. Bioorg Med Chem Lett 1999, 9, 9, 1291.
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) 27725 2-iodoaniline 615-43-0 C6H6IN 详情 详情
(II) 27726 6-methoxy-3,4-dihydro-1-naphthalenyl trifluoromethanesulfonate C12H11F3O4S 详情 详情
(III) 27727 N-(2-iodophenyl)-6-methoxy-3,4-dihydro-1-naphthalenecarboxamide C18H16INO2 详情 详情
Extended Information