Diethylamine → HCID 135856750, compound
Reaction equation
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([S:11](Cl)(=[O:13])=[O:12])=[CH:7][C:6]=1[C:15]1[NH:20][C:19](=[O:21])[C:18]2=[C:22]([CH3:28])[N:23]=[C:24]([CH2:25][CH2:26][CH3:27])[N:17]2[N:16]=1)[CH2:2][CH3:3].[CH2:29]([NH:31][CH2:32][CH3:33])[CH3:30].CN1C(=O)C2=CN=C(CCC)N2N=C1C1C(OCCC)=CC=C(S(N)(=O)=O)C=1>ClCCl.CO>[CH2:29]([N:31]([CH2:32][CH3:33])[S:11]([C:8]1[CH:9]=[CH:10][C:5]([O:4][CH2:1][CH2:2][CH3:3])=[C:6]([C:15]2[NH:20][C:19](=[O:21])[C:18]3=[C:22]([CH3:28])[N:23]=[C:24]([CH2:25][CH2:26][CH3:27])[N:17]3[N:16]=2)[CH:7]=1)(=[O:13])=[O:12])[CH3:30]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
By the same method, starting with 42 mg (0.1 mmol) of 4-propoxy-3-(5-methyl-4-oxo-7-propyl-3,4-dihydro-imidazo[5,1-f][1,2,4]triazin-2-yl)-benzenesulphonyl chloride and 22 mg (0.6 mmol) of diethylamine, 42 mg (92%) of N,N-diethyl-3-(5-(methyl-4-oxo-7-propyl-3,4-dihydro-imidazo[5,1-f][1,2,4]triazin-2-yl)-4-propoxy-benzenesulphonamide are obtained. Rf=0.64 (dichloromethane/methanol=9:1)
Workup
- customare obtained
Sources & evidence
- ORD record
- ord-6aeaf9bd407546edbed92e85626c5854
- Source dataset
- uspto-grants-2003_05
- Patent number
- US06566360B1
Reaction notes
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