Acetic Acid → HCID 66933986, compound
Reaction equation
[C:1]([OH:4])(=[O:3])[CH3:2].[Cl:5][C:6]1[CH:11]=[C:10]([Cl:12])[C:9]([F:13])=[CH:8][C:7]=1[C:14]1[O:15][C:16]2[C:21]([C:22](=[O:24])[CH:23]=1)=[C:20]([OH:25])[CH:19]=[C:18]([OH:26])[C:17]=2[C@@H:27]1[CH2:31][CH2:30][N:29]([CH3:32])[C@H:28]1[CH2:33][OH:34]>CO>[C:1]([OH:4])(=[O:3])[CH3:2].[Cl:5][C:6]1[CH:11]=[C:10]([Cl:12])[C:9]([F:13])=[CH:8][C:7]=1[C:14]1[O:15][C:16]2[C:21]([C:22](=[O:24])[CH:23]=1)=[C:20]([OH:25])[CH:19]=[C:18]([OH:26])[C:17]=2[C@@H:27]1[CH2:31][CH2:30][N:29]([CH3:32])[C@H:28]1[CH2:33][OH:34]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 52.5 °C
Procedure
Acetic acid (0.0068 g, 0.11 mmol) was added to the suspension of compound of example 47 (0.05 g, 0.11 mmol) in methanol (2 mL). It was stirred for 5 min. at 50-55° C. to get clear solution. The reaction mixture was concentrated and solid was dried to obtain the title compound.
Workup
- customto get clear solution
- concentrationThe reaction mixture was concentrated
- customsolid was dried
Sources & evidence
- ORD record
- ord-e71afc028d7b44e28e58673fcd4249af
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07884127B2
Reaction notes
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