Triethylamine → HCID 178428562, compound
Reaction equation
[N:1]1([C@H:7]2[CH2:12][CH2:11][C@H:10]([OH:13])[CH2:9][CH2:8]2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.Cl[C:15]1[N:20]=[C:19]([CH3:21])[CH:18]=[CH:17][N:16]=1.C(N(CC)CC)C>C1(C)C=CC=CC=1>[CH3:21][C:19]1[CH:18]=[CH:17][N:16]=[C:15]([N:4]2[CH2:3][CH2:2][N:1]([C@H:7]3[CH2:8][CH2:9][C@H:10]([OH:13])[CH2:11][CH2:12]3)[CH2:6][CH2:5]2)[N:20]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound 10a (4.3 g, 23.3 mmol) is placed in 100 ml of toluene in the presence of 2-chloro-4-methylpyrimidine (3 g, 23.3 mmol) and of triethylamine (4.9 ml, 35.1 mmol) and then this mixture is heated at reflux for 16 h.
Workup
- temperaturethis mixture is heated
- temperatureat reflux for 16 h.
Sources & evidence
- ORD record
- ord-3c057c410ef8429f9e6d1857a2996c85
- Source dataset
- uspto-grants-2001_02
- Patent number
- US06191130B1
Reaction notes
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