Ammonia → HCID 23295136, compound
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:5]=[C:4]([NH:13][CH2:14][CH2:15][CH2:16][CH3:17])[N:3]=1.[CH2:18]([CH:20]([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:21]N)[CH3:19].[CH2:27](N)[CH2:28][CH2:29][CH3:30].N>>[CH2:16]([CH:15]([CH2:27][CH2:28][CH2:29][CH3:30])[CH2:14][NH:13][C:4]1[N:3]=[C:2]([NH:1][CH2:21][CH:20]([CH2:18][CH3:19])[CH2:23][CH2:24][CH2:25][CH3:26])[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:5]=1)[CH3:17]Participants
5
Procedure
The same procedures were repeated as in the N-substituted melamine (C1), except that mono-2-ethylhexylamine was employed in place of n-butyl amine, and further n-butyl amine was employed in place of the aqueous ammonia to obtain 2,4-bis(mono-2-ethylhexylamino)-6-monobutylamino-1,3,5-triazine.
Sources & evidence
- ORD record
- ord-570311a6db8c4643aec31eb7f1ff7e02
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06124381
Reaction notes
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