Hydrochloric Acid → Methyl 2-Acetamido-3-[2-[(2R)-4-benzyloxycarbonyl-2-aminobutoxy]-4-cyanophenyl]acrylate Hydrochloride
Reaction equation
[C:1]([NH:4][C:5](=[CH:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]#[N:18])=[CH:13][C:12]=1[O:19][CH2:20][C@H:21]([NH:34]C(OC(C)(C)C)=O)[CH2:22][CH2:23][C:24]([O:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[O:25])[C:6]([O:8][CH3:9])=[O:7])(=[O:3])[CH3:2].[ClH:42]>O1CCOCC1>[ClH:42].[C:1]([NH:4][C:5](=[CH:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]#[N:18])=[CH:13][C:12]=1[O:19][CH2:20][C@H:21]([NH2:34])[CH2:22][CH2:23][C:24]([O:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[O:25])[C:6]([O:8][CH3:9])=[O:7])(=[O:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5 g of methyl 2-acetamido-3-[2-[(2R)-4-benzyloxycarbonyl-2-(t-butoxycarbonylamino)butoxy]-4-cyanophenyl]acrylate was stirred in 50 ml of dioxane containing 4 M of hydrogen chloride for 2 hours. The solvent was evaporated to obtain the title compound.
Workup
- customThe solvent was evaporated
Sources & evidence
- ORD record
- ord-7589d30072554d618009ff6756a2a2d2
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06710056B2
Reaction notes
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