Hydrochloric Acid → HCID 86673661, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[CH:4][N:3]=1.[N+:9]([C:12]1[CH:18]=[CH:17][C:15]([NH2:16])=[CH:14][CH:13]=1)([O-:11])=[O:10].Cl>CC(O)C>[ClH:1].[Cl:8][C:6]1[N:5]=[CH:4][N:3]=[C:2]([NH:16][C:15]2[CH:17]=[CH:18][C:12]([N+:9]([O-:11])=[O:10])=[CH:13][CH:14]=2)[CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 84 °C
Procedure
250 mg of 4,6-dichloropyrimidine and 178 mg of p-nitroaniline were dissolved in 2.5 mL of i-PrOH and 0.25 mL of 37% HCl were added. The mixture obtained was refluxed (84° C.) for 4 hours under a nitrogen atmosphere. A precipitate was formed which was collected by filtratio. 6-Chloro-N-(4-nitrophenyl)pyrimidin-4-amine hydrochloride in the form of bright yellow crystals was obtained.
Workup
- customThe mixture obtained
- customA precipitate was formed which
- customwas collected by filtratio
Sources & evidence
- ORD record
- ord-a17973f3cdd844ea81db054eb57481cc
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08986994B2
Reaction notes
Loading…