Hydrochloric Acid → HCID 67410831, compound
Reaction equation
[ClH:1].[CH3:2][O:3][C:4](=[O:22])[C@@H:5]([NH:14]C(OC(C)(C)C)=O)[CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1>>[ClH:1].[ClH:1].[CH3:2][O:3][C:4](=[O:22])[C@@H:5]([NH2:14])[CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1Participants
3
Procedure
HCl (0.45 mL of 4M in dioxane) was added to (S)-2-tert-Butoxycarbonylamino-4-piperidin-1-yl-butyric acid methyl ester and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure and dried under high vacuum for 16 hours to provide the product (46% yield).
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure
- customdried under high vacuum for 16 hours
Sources & evidence
- ORD record
- ord-29b2caa72050464187c879037eab447f
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08017641B2
Reaction notes
Loading…