Hydrochloric Acid → HCID 86742968, compound
Reaction equation
C[O:2][C:3](=[O:24])[C@:4]([N:17]([CH2:19][CH:20]([OH:23])[CH2:21][OH:22])[CH3:18])([CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=1)[N:5]=[C:6]=[O:7].Cl>O1CCOCC1.O>[CH3:18][N:17]([C@@:4]([C:3]([OH:24])=[O:2])([CH2:8][C:9]1[CH:10]=[CH:11][C:12]([O:15][CH3:16])=[CH:13][CH:14]=1)[N:5]=[C:6]=[O:7])[CH2:19][CH:20]([OH:23])[CH2:21][OH:22]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The resultant compound from Example 115 (114 mg, 0.355 mmol) in dioxane (4 ml) and water (2 ml) at 0° C. was treated with LiOH monohydrate (42.0 mg, 1 mmol). After 90 min 2M HCl (0.6 ml, 1.2 mmol) was added and the mixture was evaporated to a form which was used without further purification; DCI-MS: (M+H)+ =327.
Workup
- customthe mixture was evaporated to a form which
- customwas used without further purification
Sources & evidence
- ORD record
- ord-071184b19ab14ab184ef3d5d0bae11b4
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04826815
Reaction notes
Loading…