HCID 59864897, compound → HCID 59864864, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([O:8][C:9]2[CH:19]=[CH:18][C:12]3[N:13]=[C:14]([NH:16][CH3:17])[S:15][C:11]=3[C:10]=2[N+:20]([O-])=O)[C:5]([O:23][CH3:24])=[CH:4][C:3]=1[CH2:25][C:26]([O:28][CH3:29])=[O:27]>C(OCC)(=O)C.CO.[Pd]>[NH2:20][C:10]1[C:11]2[S:15][C:14]([NH:16][CH3:17])=[N:13][C:12]=2[CH:18]=[CH:19][C:9]=1[O:8][C:6]1[C:5]([O:23][CH3:24])=[CH:4][C:3]([CH2:25][C:26]([O:28][CH3:29])=[O:27])=[C:2]([Cl:1])[CH:7]=1Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
Compound 19.3 (230 mg, 0.53 mmol) was dissolved in mixture of ethyl acetate (3 mL) and methanol (1 mL). 10% Pd/C (56 mg, 0.053 mmol) was added and the reaction mixture was stirred for 1.5 h under H2 at room temperature. The reaction mixture was filtered, the residue concentrated under reduced pressure to afford 19.4.
Workup
- filtrationThe reaction mixture was filtered
- concentrationthe residue concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-453cb26558614bbeb124dd9ed37f28c9
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960567B2
Reaction notes
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