HCID 89995591, compound → HCID 89995631, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:13]([N:15]2[CH2:18][CH:17]([O:19][CH3:20])[CH2:16]2)=[O:14])[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)[CH3:2]>C(OCC)(=O)C.[Pd]>[NH2:10][C:9]1[CH:8]=[CH:7][C:6]([C:13]([N:15]2[CH2:18][CH:17]([O:19][CH3:20])[CH2:16]2)=[O:14])=[CH:5][C:4]=1[O:3][CH2:1][CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of (3-ethoxy-4-nitrophenyl)(3-methoxyazetidin-1-yl)methanone (Preparation 113, 230 mg, 0.821 mmol) in ethyl acetate (10 mL) was stirred with 10% palladium on charcoal under an atmosphere of hydrogen gas for 1 hour. The reaction mixture was filtered through a pad of celite, the filtrate collected and concentrated in vacuo to afford the title compound as a white solid (202 mg, 98%).
Workup
- filtrationThe reaction mixture was filtered through a pad of celite
- customthe filtrate collected
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-160143388afe43938b1c9c83008256c9
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09334286B2
Reaction notes
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