4-Tert-butylcyclohexanecarbonyl chloride → 4-tert-butyl-N-[1-(3-tert-butyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]cyclohexanecarboxamide
Reaction equation
[NH2:1][CH:2]([C:5]1[C:6](=[O:15])[NH:7][C:8]([C:11]([CH3:14])([CH3:13])[CH3:12])=[N:9][N:10]=1)[CH2:3][CH3:4].[C:16]([CH:20]1[CH2:25][CH2:24][CH:23]([C:26](Cl)=[O:27])[CH2:22][CH2:21]1)([CH3:19])([CH3:18])[CH3:17]>>[C:16]([CH:20]1[CH2:21][CH2:22][CH:23]([C:26]([NH:1][CH:2]([C:5]2[C:6](=[O:15])[NH:7][C:8]([C:11]([CH3:14])([CH3:13])[CH3:12])=[N:9][N:10]=2)[CH2:3][CH3:4])=[O:27])[CH2:24][CH2:25]1)([CH3:19])([CH3:17])[CH3:18]Participants
3
Procedure
In analogy to the procedure for Example 36A, 210 mg (1.00 mmol) 6-(1-aminopropyl)-3-tert-butyl-1,2,4-triazin-5(4H)-one, 200 mg (1.00 mmol) 4-tert-butylcyclohexanecarbonyl chloride and proportionate amounts of the other reagents are used. The crude product is used in the next step without further purification.
Workup
- customThe crude product is used in the next step without further purification
Sources & evidence
- ORD record
- ord-7430f96f69964f2dae79215de9da8d9e
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115602B2
Reaction notes
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