4-Tert-butylcyclohexanecarbonyl chloride → 4-tert-butyl-N-[1-(3-cyclopropyl-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:14])[NH:7][C:8]([CH:11]2[CH2:13][CH2:12]2)=[N:9][N:10]=1)[CH2:3][CH3:4].[C:15]([CH:19]1[CH2:24][CH2:23][CH:22]([C:25](Cl)=[O:26])[CH2:21][CH2:20]1)([CH3:18])([CH3:17])[CH3:16]>>[C:15]([CH:19]1[CH2:20][CH2:21][CH:22]([C:25]([NH:1][CH:2]([C:5]2[C:6](=[O:14])[NH:7][C:8]([CH:11]3[CH2:13][CH2:12]3)=[N:9][N:10]=2)[CH2:3][CH3:4])=[O:26])[CH2:23][CH2:24]1)([CH3:18])([CH3:16])[CH3:17]Participants
3
Procedure
In analogy to the procedure for Example 36A, 250 mg (1.29 mmol) 6-(1-aminopropyl)-3-cyclopropyl-1.2,4-triazin-5(4H)-one, 260 mg (1.29 mmol) 4-tert-butyl-cyclohexanecarbonyl 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-f368bb1ba1b14e9baf92394e9f754c20
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115602B2
Reaction notes
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