Hydrochloric Acid → HCID 59257846, compound
Reaction equation
[CH3:1][N:2]1[C:14]2[C:15]3[CH:7]([CH2:8][N:9]([CH2:16][C:17]([O:19]C(C)(C)C)=[O:18])[C:10]=3[CH:11]=[CH:12][CH:13]=2)[CH2:6][CH2:5][CH2:4][C:3]1=[O:24].Cl>CCOC(C)=O>[CH3:1][N:2]1[C:14]2[C:15]3[CH:7]([CH2:8][N:9]([CH2:16][C:17]([OH:19])=[O:18])[C:10]=3[CH:11]=[CH:12][CH:13]=2)[CH2:6][CH2:5][CH2:4][C:3]1=[O:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of tert-butyl (7-methyl-6-oxo-2a,3,4,5,6,7-hexahydroazocino[4,3,2-cd]indol-1(2H)-yl)acetate, enantiomer A, from Step G (18 mg, 0.057 mmol) in EtOAc (1 mL) was saturated with HCl (g), aged at ambient temperature for 10 min, then resaturated with HCl (g). After a further 10 min, the mixture was concentrated in vacuo to give the title compound. MS: m/z=275 (M+1).
Workup
- waitAfter a further 10 min
- concentrationthe mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-5e93670e37374309bf2a4851920f7719
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696192B2
Reaction notes
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