【结 构 式】 |
【分子编号】64801 【品名】3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-nonylpropanamide 【CA登记号】 |
【 分 子 式 】C20H28N2O3 【 分 子 量 】344.454 【元素组成】C 69.74% H 8.19% N 8.13% O 13.93% |
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)3-Phthalimidopropionyl chloride (I) is condensed with n-nonylamine to produce the corresponding amide (II). Subsequent hydrazinolysis of phthalimide (II) furnishes the aminopropanamide (III), which is condensed with D-pantonolactone (IV) to yield the desired compound.
【1】 Clifton, G.; Bryant, S.R.; Skinner, C.G.; N1-(Substituted) pantothenamides, antimetabolites of pantothenic acid. Arch Biochem Biophys 1970, 137, 2, 523. |
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) | 53390 | 3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propanoyl chloride | n/a | C11H8ClNO3 | 详情 | 详情 |
(II) | 64801 | 3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-nonylpropanamide | C20H28N2O3 | 详情 | 详情 | |
(III) | 64802 | 3-amino-N-nonylpropanamide | C12H26N2O | 详情 | 详情 | |
(IV) | 51427 | D-Pantolactone; R(-)-2-Hydroxy-3,3-dimethyl-gamma-butyrolactone | 599-04-2 | C6H10O3 | 详情 | 详情 |
Extended Information