Triethylamine → HCID 22339865, compound
Reaction equation
[Cl:1][C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:13])[CH:8]=2)[N:3]=1.[CH2:14]([NH2:24])[C:15]1[CH:23]=[CH:22][C:21]2[O:20][CH2:19][O:18][C:17]=2[CH:16]=1.C(N(CC)CC)C>C(O)(C)C>[Cl:1][C:2]1[N:11]=[C:10]([NH:24][CH2:14][C:15]2[CH:23]=[CH:22][C:21]3[O:20][CH2:19][O:18][C:17]=3[CH:16]=2)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:13])[CH:8]=2)[N:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture comprising 3.6 g of 2,4,6-trichloroquinazoline, 2.4 g of piperonylamine, 1.6 g of triethylamine and 50 ml of isopropyl alcohol was heated under reflux for 1.5 hours and hot-filtered to give 5.2 g of the title compound as a filter cake.
Workup
- temperaturewas heated
- temperatureunder reflux for 1.5 hours
- filtrationhot-filtered
Sources & evidence
- ORD record
- ord-d57fedd7f2de402dab28aa674b3de11f
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05801180
Reaction notes
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