Hydrochloric Acid → HCID 69869507, compound
Reaction equation
[C:1]1([C@@H:7]([C:12]2[C:20]3[C:15](=[CH:16][C:17]([O:21][CH2:22][CH2:23][CH2:24][NH:25][C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=4)=[CH:18][CH:19]=3)[NH:14][CH:13]=2)[CH2:8][C:9]([OH:11])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:32]>O1CCOCC1>[ClH:32].[C:1]1([C@@H:7]([C:12]2[C:20]3[C:15](=[CH:16][C:17]([O:21][CH2:22][CH2:23][CH2:24][NH:25][C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=4)=[CH:18][CH:19]=3)[NH:14][CH:13]=2)[CH2:8][C:9]([OH:11])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2 g (4.8 mmol) of the internal salt 46 are dissolved in 5 ml of dioxane and stirred for 2 hours at RT with 20 ml (20 mmol) of 1N HCl. The solution is subsequently freeze-dried, giving (3S)-3-phenyl-3-{6-[3-(pyrid in-2-ylamino)propoxy]indol-3-yl}propionic acid hydrochloride.
Workup
- customThe solution is subsequently freeze-dried
Sources & evidence
- ORD record
- ord-85b32c7d4c7f403190d0bedd9ddb99a4
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06743810B2
Reaction notes
Loading…