O-ethylhydroxylamine hydrochloride → HCID 86707232, compound
Reaction equation
[N:1]1[N:2]([C:10]2[N:31]=[CH:30][CH:29]=[CH:28][C:11]=2[C:12]([NH:14][CH:15]([CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:16]([OH:20])[C:17](O)=[O:18])=[O:13])[CH:3]=[C:4]2[C:9]=1[CH:8]=[CH:7][CH:6]=[CH:5]2.Cl.[CH2:33]([O:35][NH2:36])[CH3:34]>>[CH2:33]([O:35][NH:36][C:17](=[O:18])[CH:16]([OH:20])[CH:15]([NH:14][C:12](=[O:13])[C:11]1[CH:28]=[CH:29][CH:30]=[N:31][C:10]=1[N:2]1[CH:3]=[C:4]2[C:9]([CH:8]=[CH:7][CH:6]=[CH:5]2)=[N:1]1)[CH2:21][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)[CH3:34]Participants
3
Procedure
The reaction was carried out in analogy to reaction step 3.1 by reacting 3-[2-(2H-indazol-2-yl)nicotinamido]-2-hydroxy-4-phenylbutanoic acid and O-ethylhydroxylamine hydrochloride.
Workup
- customThe reaction was carried out in analogy to reaction step 3.1
Sources & evidence
- ORD record
- ord-b802550947f345fabd29f87dc438d9bc
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062027B2
Reaction notes
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