2,4,6-Triethyl 1,3,5-triazine-2,4,6-tricarboxylate → HCID 19831388, compound

HRID 1493391Notes

Reaction equation

HRID 1493391 reaction equation
[N:1]1[C:6]([C:7]([O:9]CC)=O)=[N:5][C:4]([C:12]([O:14]CC)=O)=[N:3][C:2]=1[C:17]([O:19]CC)=O.[CH3:22][O:23][N:24]1[C:29]([CH3:31])([CH3:30])[CH2:28][CH:27]([NH:32][CH:33]2[CH2:38][C:37]([CH3:40])([CH3:39])[N:36]([O:41][CH3:42])[C:35]([CH3:44])([CH3:43])[CH2:34]2)[CH2:26][C:25]1([CH3:46])[CH3:45]>>[CH3:42][O:41][N:36]1[C:37]([CH3:40])([CH3:39])[CH2:38][CH:33]([N:32]([CH:27]2[CH2:28][C:29]([CH3:31])([CH3:30])[N:24]([O:23][CH3:22])[C:25]([CH3:46])([CH3:45])[CH2:26]2)[C:17]([C:2]2[N:1]=[C:6]([C:7]([N:32]([CH:27]3[CH2:28][C:29]([CH3:31])([CH3:30])[N:24]([O:23][CH3:22])[C:25]([CH3:46])([CH3:45])[CH2:26]3)[CH:33]3[CH2:38][C:37]([CH3:40])([CH3:39])[N:36]([O:41][CH3:42])[C:35]([CH3:44])([CH3:43])[CH2:34]3)=[O:9])[N:5]=[C:4]([C:12]([N:32]([CH:33]3[CH2:34][C:35]([CH3:44])([CH3:43])[N:36]([O:41][CH3:42])[C:37]([CH3:40])([CH3:39])[CH2:38]3)[CH:27]3[CH2:26][C:25]([CH3:46])([CH3:45])[N:24]([O:23][CH3:22])[C:29]([CH3:30])([CH3:31])[CH2:28]3)=[O:14])[N:3]=2)=[O:19])[CH2:34][C:35]1([CH3:44])[CH3:43]

Participants

3

Reactant 2

HCID 134782,4,6-Triethyl 1,3,5-triazine-2,4,6-tricarboxylateHCID 19831392HCID 19831392, compound

Product 1

HCID 19831388HCID 19831388, compound

Procedure

The title compound is prepared by the reaction of triethyl 1,3,5-triazine-2,4,6-tricarboxylate and bis(1-methoxy-2,2,6,6-tetramethylpiperidin-4-yl)amine.

Sources & evidence

ORD record
ord-c21249ad2cd64ccdbb6726c70e7cc8e7
Source dataset
uspto-grants-1991_06
Patent number
US05021483

Reaction notes

Loading…