Hydrochloric Acid → HCID 86594427, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:21])[C@@H:4]([NH:13]C(OC(C)(C)C)=O)[CH2:5][CH2:6][N:7]([CH2:9][CH2:10][O:11][CH3:12])[CH3:8].[ClH:22]>>[ClH:22].[ClH:22].[CH3:1][O:2][C:3](=[O:21])[C@@H:4]([NH2:13])[CH2:5][CH2:6][N:7]([CH2:9][CH2:10][O:11][CH3:12])[CH3:8]Participants
3
Procedure
(S)-2-tert-Butoxycarbonylamino-4-[(2-methoxyethyl)-methylamino]-butyric acid methyl ester (0.086 g, 0.28 mmol) was treated with HCl (1 mL of 4M in dioxane) and sonicated. The mixture was concentrated and dried under high vacuum to provide the product.
Workup
- customsonicated
- concentrationThe mixture was concentrated
- customdried under high vacuum
- customto provide the product
Sources & evidence
- ORD record
- ord-c61b1ba44a41445485bcc6c9346e342e
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08518983B2
Reaction notes
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