Hydrochloric Acid → HCID 86589657, compound
Reaction equation
C([O:8][C:9](=[O:28])[CH:10]([NH:20]C(OC(C)(C)C)=O)[CH2:11][NH:12]C(OC(C)(C)C)=O)C1C=CC=CC=1.[ClH:29]>C(#N)C>[ClH:29].[ClH:29].[ClH:29].[NH2:20][CH:10]([CH2:11][NH2:12])[C:9]([OH:28])=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2,3-bis-tert-butoxycarbonylamino propionic acid benzyl ester (1.8 g), 4N aqueous HCl (40 ml), and acetonitrile (50 ml) was stirred for 18 hours at room temperature. The solvent was removed under vacuum, and the mixture was diluted with ethyl acetate (100 ml) and water (50 ml) and stirred for 15 minutes. The layers were separated and the aqueous layer was evaporated to dryness (1.23 g of a foam/syrup). 1H NMR (300 MHz): 3.2-3.5 (m, 2H), 4.2-4.35 (m, 1H), 5.13-5.25 (q, 2H, J=11.8, 3.1 Hz).
Workup
- customThe solvent was removed under vacuum
- additionthe mixture was diluted with ethyl acetate (100 ml) and water (50 ml)
- customThe layers were separated
- customthe aqueous layer was evaporated to dryness (1.23 g of a foam/syrup)
Sources & evidence
- ORD record
- ord-423113c6f9214254b81f248800c52937
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07238341B2
Reaction notes
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