Hydrochloric Acid → HCID 58012031, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([CH2:13][CH2:14][CH2:15][C:16]([O:18]C(C)(C)C)=[O:17])[C:11](=[O:23])[N:10]([CH2:24][C:25]([NH:27][CH2:28][C:29]([CH3:41])([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=3[C:37]([F:40])([F:39])[F:38])[CH3:30])=[O:26])[N:9]=2)=[CH:4][CH:3]=1.Cl>O1CCOCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17])[C:11](=[O:23])[N:10]([CH2:24][C:25]([NH:27][CH2:28][C:29]([CH3:41])([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=3[C:37]([F:38])([F:39])[F:40])[CH3:30])=[O:26])[N:9]=2)=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound from Example 365 (22 mg, 37 μmol) is stirred overnight at RT with 1 ml of a 4 M hydrogen chloride solution in dioxan. The solvent is then removed on the rotary evaporator. The residue is taken up in DMSO and purified by preparative HPLC (Method 20). 14 mg (70% of theory) of the title compound are obtained.
Workup
- customThe solvent is then removed on the rotary evaporator
- custompurified by preparative HPLC (Method 20)
Sources & evidence
- ORD record
- ord-18979c944aec4eedaa5ab673afe99b7d
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084481B2
Reaction notes
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