Hydrochloric Acid → HCID 66727689, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C@@H:8]([NH2:11])[CH2:9][CH3:10])[CH:3]=1.C(=O)(O)[O-].[Na+].[ClH:17]>>[ClH:17].[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C@@H:8]([NH2:11])[CH2:9][CH3:10])[CH:3]=1Participants
4
Procedure
A mixture of (S)-1-(4-bromopyridin-2-yl)-propylamine (0.600 g, 1.88 mmol) in 3 N aqueous HCl is stirred for 16 hours. The mixture is then added to a solution of saturated aqueous sodium bicarbonate (15 mL) and extracted with EtOAc (5×15 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated in vacuo to afford the title compound which is used without purification.
Workup
- extractionextracted with EtOAc (5×15 mL)
- dry with materialThe combined organic layers are dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-6d0e4efa93054fe1b5bccb118450cbe5
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08927550B2
Reaction notes
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