Ammonia → HCID 23292945, compound

HRID 1955171Notes

Reaction equation

HRID 1955171 reaction equation
N[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.[NH:18]1[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1.N>>[CH2:14]([NH:13][C:4]1[N:5]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:7]=[C:2]([N:18]2[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)[N:3]=1)[CH2:15][CH2:16][CH3:17]

Participants

4

Reactant 3

HCID 222AmmoniaHCID 8082PiperidineHCID 11806705HCID 11806705, compound

Product 1

HCID 23292945HCID 23292945, compound

Procedure

The same procedures were repeated as in the N-substituted melamine (C1), except that piperidine was employed in place of the aqueous ammonia to obtain 2,4-bis(monobutylamino)-6-piperidino-1,3,5-triazine which is in powder-state.

Sources & evidence

ORD record
ord-f19decbcf8ff441aa735ef9e61021517
Source dataset
uspto-grants-2000_09
Patent number
US06124381

Reaction notes

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