MI-773 → SAR405838 (MI-773)
Reaction equation
[CH3:1][C:2]([CH2:5][C@H:6]1[NH:10][C@@H:9]([C:11]([NH:13][CH:14]2[CH2:19][CH2:18][CH:17]([OH:20])[CH2:16][CH2:15]2)=[O:12])[C@H:8]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([Cl:27])[C:22]=2[F:28])[C@:7]21[C:37](=[O:38])[NH:36][C:30]1[CH:31]=[C:32]([Cl:35])[CH:33]=[CH:34][C:29]2=1)([CH3:4])[CH3:3]>CO.O>[CH3:4][C:2]([CH2:5][C@@H:6]1[NH:10][C@@H:9]([C:11]([NH:13][CH:14]2[CH2:15][CH2:16][CH:17]([OH:20])[CH2:18][CH2:19]2)=[O:12])[C@H:8]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([Cl:27])[C:22]=2[F:28])[C@@:7]21[C:37](=[O:38])[NH:36][C:30]1[CH:31]=[C:32]([Cl:35])[CH:33]=[CH:34][C:29]2=1)([CH3:1])[CH3:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
In an alternative procedure, MI-773 (77 mg) was dissolved in 15 mL MeOH/H2O (v/v=1:1). After 3 days, the needle crystals that had formed were collected, washed with cold MeOH/H2O (v/v=1:1) and dried in vacuum to give MI-77301 as the free amine (20 mg; >95% purity as determined by HPLC).
Workup
- customthe needle crystals that had formed
- customwere collected
- washwashed with cold MeOH/H2O (v/v=1:1)
- customdried in vacuum
Sources & evidence
- ORD record
- ord-6d33354d2ad248e29d949c4d824d277f
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877796B2
Reaction notes
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