Tert-Butylamine → HCID 19073890, compound
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[C:4](Cl)[N:3]=1.[C:10]([NH2:14])([CH3:13])([CH3:12])[CH3:11]>C(O)C>[NH2:1][C:2]1[N:3]=[C:4]([NH:14][C:10]([CH3:13])([CH3:12])[CH3:11])[CH:5]=[C:6]([Cl:8])[N:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
10 g of 2-amino-4,6-dichloropyrimidine are suspended in 100 ml of ethanol. 44.50 g of tert-butylamine are added. The reaction mixture is refluxed for 48 hours. It is evaporated to dryness. The residue is taken up in 50 ml of water. The mixture is stirred for 1 hour and the precipitate is then filtered off on sintered glass. It is recrystallized from 60 ml of a 50/50 ethanol-water mixture. 9.25 g of 2-amino-4-tert-butylamino-6-chloro-pyrimidine are obtained.
Workup
- temperatureThe reaction mixture is refluxed for 48 hours
- customIt is evaporated to dryness
- filtrationthe precipitate is then filtered off on sintered glass
- customIt is recrystallized from 60 ml of a 50/50 ethanol-water mixture
Sources & evidence
- ORD record
- ord-29e44f8b4727462982e7717f2fd6a3b3
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05772990
Reaction notes
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