Cyclohexane → HCID 53759049, compound

HRID 133637Notes

Reaction equation

[OH:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([CH2:10][CH2:11][CH2:12][CH2:13][NH:14][C:15]2[N:20]=[C:19]([NH:21][CH2:22][CH2:23][CH2:24][CH2:25][CH:26]3[CH2:31][C:30]([CH3:33])([CH3:32])[N:29]([OH:34])[C:28]([CH3:36])([CH3:35])[CH2:27]3)[N:18]=[C:17]([NH:37][CH2:38][CH2:39][CH2:40][CH2:41][CH:42]3[CH2:47][C:46]([CH3:49])([CH3:48])[N:45]([OH:50])[C:44]([CH3:52])([CH3:51])[CH2:43]3)[N:16]=2)[CH2:4][C:3]1([CH3:54])[CH3:53].[CH2:55]1[CH2:60][CH2:59][CH2:58][CH2:57][CH2:56]1>>[CH:55]1([O:50][N:45]2[C:44]([CH3:52])([CH3:51])[CH2:43][CH:42]([CH2:41][CH2:40][CH2:39][CH2:38][NH:37][C:17]3[N:16]=[C:15]([NH:14][CH2:13][CH2:12][CH2:11][CH2:10][CH:5]4[CH2:4][C:3]([CH3:54])([CH3:53])[N:2]([O:1][CH:55]5[CH2:60][CH2:59][CH2:58][CH2:57][CH2:56]5)[C:7]([CH3:9])([CH3:8])[CH2:6]4)[N:20]=[C:19]([NH:21][CH2:22][CH2:23][CH2:24][CH2:25][CH:26]4[CH2:31][C:30]([CH3:32])([CH3:33])[N:29]([O:34][CH:55]5[CH2:60][CH2:59][CH2:58][CH2:57][CH2:56]5)[C:28]([CH3:36])([CH3:35])[CH2:27]4)[N:18]=3)[CH2:47][C:46]2([CH3:49])[CH3:48])[CH2:60][CH2:59][CH2:58][CH2:57][CH2:56]1

Participants

Reactant 2

HCID 8078Cyclohexane

HCID 69201187HCID 69201187, compound

Product 1

HCID 53759049HCID 53759049, compound

Procedure

The title compound is prepared from the reaction of 2,4,6-tris[N-(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-s-triazine and cyclohexane following a procedure similar to that of Example 10.

Sources & evidence

ORD record: ord-f35ec68f634143d9813a90e16598c328
Source dataset: uspto-grants-2008_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07390904B2

Reaction notes

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