Hydroxylamine → HCID 86653953, compound
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:16][CH2:15][O:14][C@H:13]([C@@H:17]([OH:30])[C:18]([NH:20][C:21]3[CH:26]=[CH:25][C:24]([C:27]#[N:28])=[CH:23][C:22]=3[Cl:29])=[O:19])[C:12]2=[O:31])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[NH2:32][OH:33]>CCO>[C:1]([C:5]1[CH:6]=[CH:7][C:8]([N:11]2[CH2:16][CH2:15][O:14][C@H:13]([C@@H:17]([OH:30])[C:18]([NH:20][C:21]3[CH:26]=[CH:25][C:24]([C:27](=[N:32][OH:33])[NH2:28])=[CH:23][C:22]=3[Cl:29])=[O:19])[C:12]2=[O:31])=[CH:9][CH:10]=1)([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of compound 66-1 (60 mg) in EtOH (2 mL), was added 50% NH2OH aq. (22.4 microL). The reaction mixture was stirred at room temperature overnight. Then the mixture was concentrated in vacuo to obtain compound 66-2 (67 mg) as a colorless amorphous solid.
Workup
- concentrationThen the mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-35852d5b1e154766af4620bc6069db2b
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987242B2
Reaction notes
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