Hydrochloric Acid → HCID 18784789, compound
Reaction equation
[F:1][C:2]([F:40])([F:39])[CH2:3][NH:4][C:5]([C:7]1([CH2:20][CH2:21][NH:22][C:23]([N:25]2[CH2:30][CH2:29][CH:28]([NH:31][C:32](=O)[O:33]C(C)(C)C)[CH2:27][CH2:26]2)=[O:24])[C:19]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[C:13]2[C:8]1=[CH:9][CH:10]=[CH:11][CH:12]=2)=[O:6].Cl.O1[CH2:47][CH2:46]OCC1>C1COCC1>[C:32]([NH:31][CH:28]1[CH2:29][CH2:30][N:25]([C:23]([NH:22][CH2:21][CH2:20][C:7]2([C:5]([NH:4][CH2:3][C:2]([F:40])([F:39])[F:1])=[O:6])[C:19]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[C:13]3[C:8]2=[CH:9][CH:10]=[CH:11][CH:12]=3)=[O:24])[CH2:26][CH2:27]1)(=[O:33])[C:47]1[CH:46]=[CH:9][CH:8]=[CH:7][CH:5]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of Example 487 compound (1.1 g, 1.97 mmol) in THF (4 mL) was added 4N HCl in dioxane (9 mL, 36.4 mmol). The reaction mixture was stirred at room temperature for 3 h and concentrated in vacuo and then from dioxane (3×10 mL) to give crude title compound (1.46 g) as a white foamy solid.
Workup
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-73d104432e0a4ad492e4524ea5d71af0
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05739135
Reaction notes
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