HCID 23144724, compound → HCID 23144103, compound
Reaction equation
Cl[C:2]1[N:7]=[CH:6][N:5]=[C:4]([N:8]2[CH2:13][CH2:12][CH:11]([C:14]([NH:16][C:17]3[S:18][C:19]([N:27]4[CH2:32][CH2:31][O:30][CH2:29][CH2:28]4)=[C:20]([C:22]4[O:23][CH:24]=[CH:25][CH:26]=4)[N:21]=3)=[O:15])[CH2:10][CH2:9]2)[CH:3]=1.[H][H]>C(O)C.[C].[Pd]>[O:23]1[CH:24]=[CH:25][CH:26]=[C:22]1[C:20]1[N:21]=[C:17]([NH:16][C:14]([CH:11]2[CH2:10][CH2:9][N:8]([C:4]3[CH:3]=[CH:2][N:7]=[CH:6][N:5]=3)[CH2:13][CH2:12]2)=[O:15])[S:18][C:19]=1[N:27]1[CH2:32][CH2:31][O:30][CH2:29][CH2:28]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Compound 51 (300 mg, 0.63 mmol) was dissolved in ethanol (10 mL), and 10% palladium-carbon (500 mg) was added thereto, followed by stirring in an atmosphere of hydrogen at room temperature for 4 hours. The reaction mixture was filtered through Celite, and the filtrate was distilled away under reduced pressure to afford the entitled Compound 52 (213 mg, 77%).
Workup
- filtrationThe reaction mixture was filtered through Celite
- distillationthe filtrate was distilled away under reduced pressure
Sources & evidence
- ORD record
- ord-2854f194c80e4417a06083f15680f51a
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07880013B2
Reaction notes
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