Hydrogen chloride-ethyl acetate → HCID 68421306, compound
Reaction equation
[CH:1]1[C:11]2[CH:10]=[CH:9][C:8]3[CH:12]=[CH:13][CH:14]=[CH:15][C:7]=3[C:6](=[C:16]3[CH2:21][CH2:20][N:19]([C:22](=[O:40])[C@@H:23]([NH:32]C(=O)OC(C)(C)C)[CH2:24][NH:25][C:26](=[O:31])[C:27]([CH3:30])([CH3:29])[CH3:28])[CH2:18][CH2:17]3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[ClH:41].C(OCC)(=O)C>C(OCC)(=O)C>[ClH:41].[NH2:32][C@H:23]([C:22]([N:19]1[CH2:18][CH2:17][C:16](=[C:6]2[C:5]3[CH:4]=[CH:3][CH:2]=[CH:1][C:11]=3[CH:10]=[CH:9][C:8]3[CH:12]=[CH:13][CH:14]=[CH:15][C:7]2=3)[CH2:21][CH2:20]1)=[O:40])[CH2:24][NH:25][C:26](=[O:31])[C:27]([CH3:30])([CH3:29])[CH3:28]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.40 g (2.57 mmol) of the compound obtained in step 1 described above was dissolved in 12 ml of ethyl acetate. 10 ml of 4 N hydrochloric acid/ethyl acetate was added to the obtained solution under cooling with ice. The temperature was gradually elevated to room temperature. After stirring for 3.5 hours, the solvent was evaporated under reduced pressure to obtain the title compound.
Workup
- temperatureunder cooling with ice
- customwas gradually elevated to room temperature
- customthe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-551172fd65c64dfb8a6363dec927ad9b
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07462630B2
Reaction notes
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