Triethylamine → HCID 86668819, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([Cl:8])[N:5]=[C:4]([NH:9][C:10]2[CH:15]=[CH:14][C:13]([P:16]([CH3:19])([CH3:18])=[O:17])=[CH:12][CH:11]=2)[N:3]=1.C(N(CC)CC)C.[C:27]12([CH2:37][NH2:38])[CH2:36][CH:31]3[CH2:32][CH:33]([CH2:35][CH:29]([CH2:30]3)[CH2:28]1)[CH2:34]2>C(O)C>[Cl:8][C:6]1[N:5]=[C:4]([NH:9][C:10]2[CH:15]=[CH:14][C:13]([P:16]([CH3:19])([CH3:18])=[O:17])=[CH:12][CH:11]=2)[N:3]=[C:2]([NH:38][CH2:37][C:27]23[CH2:36][CH:31]4[CH2:30][CH:29]([CH2:35][CH:33]([CH2:32]4)[CH2:34]2)[CH2:28]3)[N:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 4,6-dichloro-N-[4-(dimethylphosphoryl)phenyl]-1,3,5-triazin-2-amine (0.072 mmol) in 1.5 mL of ethanol is added 10 μL of triethylamine and 1-(1-adamantyl)-methanamine (7.2 mg, 0.072 mmol). The mixture can be microwaved at 120 degrees for 20 minutes. The reaction mixture is filtered through a syringe filter and purified by prep-HPLC.
Workup
- customThe mixture can be microwaved at 120 degrees for 20 minutes
- filtrationThe reaction mixture is filtered through a syringe
- filtrationfilter
- custompurified by prep-HPLC
Sources & evidence
- ORD record
- ord-54434e2d9b9c45bb968ea53b19bdf1a9
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09012462B2
Reaction notes
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