Hydroxyamine hydrochloride → HCID 86759748, compound
Reaction equation
[NH2:1][CH:2]([CH2:6][CH2:7][C:8](=[O:30])[NH:9][CH:10]([C:23](=[O:29])[NH:24][CH2:25][C:26]([OH:28])=[O:27])[CH2:11][S:12][CH2:13][C:14]([C:16]([O:18][CH2:19][CH2:20]CC)=[O:17])=O)[C:3]([OH:5])=[O:4].Cl.[NH2:32][OH:33]>>[NH2:1][CH:2]([CH2:6][CH2:7][C:8](=[O:30])[NH:9][CH:10]([C:23](=[O:29])[NH:24][CH2:25][C:26]([OH:28])=[O:27])[CH2:11][S:12][CH2:13][C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[N:32][OH:33])[C:3]([OH:5])=[O:4]Participants
3
Procedure
Similarly, by following the procedure of Example 30A and substituting 2-amino-4-[1-(carboxymethyl-carbamoyl)-2-(2-ethoxycarbonyl-2-oxo-ethylsulfanyl)-ethylcarbamoyl]-butyric acid with 2-amino-4-[2-(2-butoxycarbonyl-2-oxo-ethylsulfanyl)-1-(carboxymethyl-carbamoyl)-ethylcarbamoyl]-butyric acid and hydroxylamine HCl with another substituted hydroxylamine there are obtained the following compounds:
Workup
- customare obtained the following compounds
Sources & evidence
- ORD record
- ord-ec8923edb6754ca88b3b84d6451bedc6
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06916850B2
Reaction notes
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