Nitric Acid → 7-Chloro-9-nitro-beta-carboline

HRID 1393981Notes

Reaction equation

HRID 1393981 reaction equation
[Cl:1][C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[CH:7]=[CH:8][N:9]=[CH:10][C:11]=3[NH:12]2)=[CH:4][CH:3]=1.O.[N+:16]([O-])([OH:18])=[O:17]>>[Cl:1][C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[CH:7]=[CH:8][N:9]=[CH:10][C:11]=3[N:12]2[N+:16]([O-:18])=[O:17])=[CH:4][CH:3]=1

Participants

4

Procedure

A mixture of the product from example 12 (500 mg, 2.48 mmol) in concentrated nitric acid (20 ml) was stirred at RT for 22 h. The reaction mixture was carefully poured into cold (3° C. to 5° C.) water (50 ml), and after stirring for 2 h the precipitate was collected. The solid was suspended in saturated aqueous NaHCO3 (50 ml) and stirred at RT for 12 h. The product was filtered and washed with water to provide 550 mg of 7-chloro-9-nitro-β-carboline

Workup

  1. stirringafter stirring for 2 h the precipitate
  2. customwas collected
  3. stirringstirred at RT for 12 h
  4. filtrationThe product was filtered
  5. washwashed with water

Sources & evidence

ORD record
ord-6aba23af214d487c9f7488fbc32aae67
Source dataset
uspto-grants-2008_03
Patent number
US07348336B2

Reaction notes

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