Hydrogen chloride-ethyl acetate → HCID 131734860, compound
Reaction equation
C(OC([NH:8][C@@H:9]([CH2:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][CH2:26][C:27]#[C:28][CH3:29])=[CH:21][CH:20]=1)[C:10]([NH:12][CH2:13][C:14]([O:16][CH3:17])=[O:15])=[O:11])=O)(C)(C)C.[ClH:30].C(OCC)(=O)C>C(OCC)(=O)C>[ClH:30].[NH2:8][C@@H:9]([CH2:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][CH2:26][C:27]#[C:28][CH3:29])=[CH:21][CH:20]=1)[C:10]([NH:12][CH2:13][C:14]([O:16][CH3:17])=[O:15])=[O:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl [(S)-2-tert-butoxycarbonylamino-3-(4-but-2-ynyloxy-phenyl)-propionylamino]-acetate (141 mg, 0.349 mmol) was dissolved in ethyl acetate (2.0 mL), and 4 M hydrogen chloride/ethyl acetate (0.2 mL) was added. The mixture was stirred at room temperature for 18 hours.
Sources & evidence
- ORD record
- ord-7266883a18384f01949e4becd1dd8630
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266853B2
Reaction notes
Loading…