反应 #742282

ord-04578813cb134c4ea0b7bcdc111c57e0

反应方程式

CC1=Nc2ccc3cc(S(=O)(=O)[O-])ccc3c2C1(C)C.[K+]
potassium 1,1,2-trimethyl-1H-benzo[e]indole-7-sulfonate
O=C(O)CCCCBr
5-bromovaleric acid
CC1=[N+](CCCCC(=O)O)c2ccc3cc(S(=O)(=O)[O-])ccc3c2C1(C)C
3-(4-carboxybutyl)-1,1,2-trimethyl-1H-benzo[e]indolium-7-sulfonate
收率 7.2%

反应条件

温度
140°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Removal of the solvent and purification by chromatography (dichloromethane/methanol)

实验过程

To a solution of 1,1,2-trimethyl-1H-benzo[e]indole-7-sulfonic acid (723 mg, 2.5 mmol) in methanol (5 mL) was added a saturated solution of potassium hydroxide in isopropanol (3.134%, 4.913 g, 1.1 eq.) and the resulting suspension was heated at reflux for 2 h. Then the mixture was concentrated and the corresponding potassium salt was obtained. Under nitrogen atmosphere, a mixture of potassium 1,1,2-trimethyl-1H-benzo[e]indole-7-sulfonate and 5-bromovaleric acid (585 mg, 3 mmol) in 3-methyl-2-butanone (5 mL) was heated at 140° C. for 20 h. Removal of the solvent and purification by chromatography (dichloromethane/methanol) afforded 3-(4-carboxybutyl)-1,1,2-trimethyl-1H-benzo[e]indolium-7-sulfonate (70 mg, isolated yield 7.2%). LC-MS: 390.18 [M+].

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08071388B2uspto-grants-2011_12