Ethyl bromoacetate → HCID 90093751, compound
Reaction equation
[CH:1]([C:4]1[NH:8][N:7]=[CH:6][CH:5]=1)([CH3:3])[CH3:2].Br[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]>>[CH2:14]([O:13][C:11](=[O:12])[CH2:10][N:8]1[C:4]([CH:1]([CH3:3])[CH3:2])=[CH:5][CH:6]=[N:7]1)[CH3:15]Participants
3
Procedure
Prepared according to the method described for Preparation 75 using 5-isopropyl-1H-pyrazole and ethyl bromoacetate. The residue was purified using silica gel column chromatography eluting with 4:1 hexane:EtOAc. The title compound was isolated as the lower running minor product in 6% yield, and taken directly on to the next step.
Workup
- customPrepared
- customThe residue was purified
- washeluting with 4:1 hexane
Sources & evidence
- ORD record
- ord-d7ba6912db9b4940affd182c946499f4
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09163021B2
Reaction notes
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