Pentanenitrile, 4,4-dimethyl-3-oxo- → HCID 58851621, compound
Reaction equation
[CH3:1][C:2]([CH3:9])([CH3:8])[C:3](=O)[CH2:4][C:5]#[N:6].Cl.[CH2:11]([O:18][C:19]1[CH:24]=[CH:23][C:22]([NH:25][NH2:26])=[CH:21][CH:20]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[CH2:11]([O:18][C:19]1[CH:20]=[CH:21][C:22]([N:25]2[C:5]([NH2:6])=[CH:4][C:3]([C:2]([CH3:9])([CH3:8])[CH3:1])=[N:26]2)=[CH:23][CH:24]=1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1Participants
3
Procedure
The title compound was prepared from 4,4-dimethyl-3-oxopentane nitrile and 4-benzyloxyphenylhydrazine hydrochloride, using the same method as that described for preparation 7, as a pale pink powder in quantitative yield.
Workup
- customthat described for preparation 7, as a pale pink powder in quantitative yield
Sources & evidence
- ORD record
- ord-7ae1c945f3514849b65891563ac7b624
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08076356B2
Reaction notes
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