反应 #40483

ord-6cee690533f34e0b838930aeaf183eee

反应方程式

C
charcoal
CN(C)CCSc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
[2-(6-chloro-8-nitro-9H-β-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amine
[Cl-].[NH4+]
ammonium chloride
CN(C)CCSc1c(Cl)cc2c([nH]c3cnccc32)c1N
6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-β-carbolin-8-ylamine
收率 107.0%

反应条件

温度
60°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度Next, the mixture was cooled to RT
  2. 2
    workup.ADDITIONwas added
  3. 3
    过滤The resulting mixture was filtered through a pad of celite
  4. 4
    浓缩the resulting filtrate concentrated

实验过程

A 50 ml round-bottom flask with a magnetic stirrer was charged with [2-(6-chloro-8-nitro-9H-β-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amine (106 mg, 0.30 mmol) in 8 ml of anhydrous ethanol. To the resulting orange mixture at RT was added 0.33 M aqueous ammonium chloride (1.95 ml, 0.64 mmol) and iron powder (540 mg, 9.67 mmol). The reaction mixture was heated to 60° C. and stirred vigorously for 20 hr. Next, the mixture was cooled to RT, diluted with ethyl acetate (20 ml) and activated charcoal (ca. 150 mg) was added. The resulting mixture was filtered through a pad of celite and the resulting filtrate concentrated to afford 103 mg of 6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-β-carbolin-8-ylamine as a yellow solid. The crude product was used directly in the coupling step.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07727985B2uspto-grants-2010_06