Hydrochloric Acid → HCID 69520324, compound
Reaction equation
[C:1]([C:3]1[C:4]([S:10][C@@H:11]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH2:12][NH:13]C(=O)OC(C)(C)C)=[N:5][C:6]([CH3:9])=[CH:7][CH:8]=1)#[N:2].[ClH:27]>O1CCOCC1>[ClH:27].[NH2:13][CH2:12][C@@H:11]([S:10][C:4]1[C:3]([C:1]#[N:2])=[CH:8][CH:7]=[C:6]([CH3:9])[N:5]=1)[C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product from step (c) (45 mg) was dissolved in 4M HCl in dioxane (5 ml). The resulting solution was stirred at room temperature for 15 minutes, then the solvent was evaporated off. The residue was recrystallised from diethyl ether/ethanol to give the title compound as a white solid (19 mg).
Workup
- customthe solvent was evaporated off
- customThe residue was recrystallised from diethyl ether/ethanol
Sources & evidence
- ORD record
- ord-101fdc1c64be4175a6927b9a5eabfeda
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07223794B2
Reaction notes
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