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【结 构 式】

【分子编号】22068

【品名】2-[1,2-diamino-2-(2-hydroxyphenyl)ethyl]phenol

【CA登记号】

【 分 子 式 】C14H16N2O2

【 分 子 量 】244.29332

【元素组成】C 68.83% H 6.6% N 11.47% O 13.1%

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:(IV)

meso-1,2-Bis(2,6-dichloro-4-hydroxyphenyl)ethylenediamine (I) is svnthesized by [3.3]sigmatropic diaza-Cope rearrangement according to the method of Vögtle and Goldschmitt by reaction of meso-1,2-bis(2-hydroxyphenyl)ethylenediamine (IV) with 2,6-dichloro-4methoxybenzaldehyde (V) at temperature below 120 C via the corresponding aldimine (VI) and subsequent ether cleavage with boron tribromide.

1 Vogtle, F.; Goldschmidt, E.; Chem Ber 1976, 109, 1.
2 Lux, F.; Hilgard, P.; Respondek, J.M.; Karl, J.; Engel, J.; Schonenberger, H.; Schumacher, W.; D-19384. Drugs Fut 1988, 13, 3, 215.
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) 22066 3,5-dichloro-4-[1,2-diamino-2-(2,6-dichloro-4-hydroxyphenyl)ethyl]phenol C14H12Cl4N2O2 详情 详情
(IV) 22068 2-[1,2-diamino-2-(2-hydroxyphenyl)ethyl]phenol C14H16N2O2 详情 详情
(V) 22069 2,6-dichloro-4-methoxybenzaldehyde C8H6Cl2O2 详情 详情
(VI) 22070 2-[[(1,2-bis(2,6-dichloro-4-methoxyphenyl)-2-[[(E)-(2-hydroxyphenyl)methylidene]amino]ethyl)imino]methyl]phenol C30H24Cl4N2O4 详情 详情
(VII) 22071 2-[1,2-bis[[(E)-(2,6-dichloro-4-methoxyphenyl)methylidene]amino]-2-(2-hydroxyphenyl)ethyl]phenol C30H24Cl4N2O4 详情 详情
(VIII) 22072 1,2-bis(2,6-dichloro-4-methoxyphenyl)-1,2-ethanediamine; 2-amino-1,2-bis(2,6-dichloro-4-methoxyphenyl)ethylamine C16H16Cl4N2O2 详情 详情
(IX) 21351 2-Hydroxybenzaldehyde;Salicylic aldehyde;2-Formylphenol;salicylaldehyde 90-02-8 C7H6O2 详情 详情
Extended Information