Ethanol hydrochloride → HCID 178472547, compound
Reaction equation
[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][C:14]([NH:16][C@H:17]([C:24]([OH:26])=[O:25])[CH2:18][C:19]1[N:23]=[CH:22][NH:21][CH:20]=1)=[O:15])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:27](O)[CH3:28].Cl>C(O)C>[CH2:27]([O:25][C:24](=[O:26])[C@H:17]([CH2:18][C:19]1[N:23]=[CH:22][NH:21][CH:20]=1)[NH:16][C:14](=[O:15])[CH2:13][CH2:12][NH:11][C:9]([O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:10])[CH3:28]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 1 L round-bottom flask, under nitrogen atmosphere, is loaded with 40 g of 3-(benzyloxycarbonylamino) propionyl-L-histidine, 200 g of absolute ethanol and 80 g of an 8M HCl ethanol solution.
Sources & evidence
- ORD record
- ord-48b6915fe4514c7cb20975e969c22d5f
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08623900B2
Reaction notes
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