Ethyl 4-chloro-2,6-dimethylnicotinate → Ethyl 2,6-dimethyl-4-[2-methyl-3-(4-tert-butylcyclohexyl)propylamino]nicotinate

HRID 266108Notes

Reaction equation

HRID 266108 reaction equation
Cl[C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:6]([CH3:13])[N:5]=[C:4]([CH3:14])[CH:3]=1.[CH3:15][CH:16]([CH2:19][CH:20]1[CH2:25][CH2:24][CH:23]([C:26]([CH3:29])([CH3:28])[CH3:27])[CH2:22][CH2:21]1)[CH2:17][NH2:18]>>[CH3:13][C:6]1[N:5]=[C:4]([CH3:14])[CH:3]=[C:2]([NH:18][CH2:17][CH:16]([CH3:15])[CH2:19][CH:20]2[CH2:21][CH2:22][CH:23]([C:26]([CH3:29])([CH3:28])[CH3:27])[CH2:24][CH2:25]2)[C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9]

Participants

3

Reactant 2

HCID 239536Ethyl 4-chloro-2,6-dimethylnicotinateHCID 190325512-Methyl-3-(4-tert-butylcyclohexyl)propylamine

Product 1

HCID 19032595Ethyl 2,6-dimethyl-4-[2-methyl-3-(4-tert-butylcyclohexyl)propylamino]nicotinate

Procedure

was synthesized analogously to Example 8 using ethyl 4-chloro-2,6-dimethylnicotinate and 2-methyl-3-(4-tert-butylcyclohexyl)propylamine nD23 :1.4738.

Sources & evidence

ORD record
ord-b60d5614fde8496c928e10ec7528fd7c
Source dataset
uspto-grants-1997_07
Patent number
US05650417

Reaction notes

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