4-Tert-butylcyclohexanecarbonyl chloride → 4-tert-butyl-N-[1-(3-cyclopentyl-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:16])[NH:7][C:8]([CH:11]2[CH2:15][CH2:14][CH2:13][CH2:12]2)=[N:9][N:10]=1)[CH2:3][CH3:4].[C:17]([CH:21]1[CH2:26][CH2:25][CH:24]([C:27](Cl)=[O:28])[CH2:23][CH2:22]1)([CH3:20])([CH3:19])[CH3:18]>>[C:17]([CH:21]1[CH2:22][CH2:23][CH:24]([C:27]([NH:1][CH:2]([C:5]2[C:6](=[O:16])[NH:7][C:8]([CH:11]3[CH2:15][CH2:14][CH2:13][CH2:12]3)=[N:9][N:10]=2)[CH2:3][CH3:4])=[O:28])[CH2:25][CH2:26]1)([CH3:20])([CH3:18])[CH3:19]Participants
3
Procedure
In analogy to the procedure for Example 36A, 200 mg (0.90 mmol) 6-(1-aminopropyl)-3-cyclopentyl-1,2,4-triazin-5(4H)-one, 180 mg (0.90 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-d501e2c2584c40d793b94f1406f021a7
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115602B2
Reaction notes
Loading…