HCID 86618889, compound → HCID 86618888, compound
Reaction equation
[N:1]([CH2:4][CH:5]([CH:7]([NH:29][C:30](=[O:36])[O:31][C:32]([CH3:35])([CH3:34])[CH3:33])[CH2:8][CH:9]([CH2:13][C:14]1[CH:15]=[C:16]2[C:20](=[CH:21][CH:22]=1)[N:19]([CH3:23])[CH:18]=[C:17]2[CH2:24][CH2:25][CH2:26][O:27][CH3:28])[CH:10]([CH3:12])[CH3:11])[OH:6])=[N+]=[N-]>CO.[Pd]>[NH2:1][CH2:4][CH:5]([CH:7]([NH:29][C:30](=[O:36])[O:31][C:32]([CH3:33])([CH3:35])[CH3:34])[CH2:8][CH:9]([CH2:13][C:14]1[CH:15]=[C:16]2[C:20](=[CH:21][CH:22]=1)[N:19]([CH3:23])[CH:18]=[C:17]2[CH2:24][CH2:25][CH2:26][O:27][CH3:28])[CH:10]([CH3:11])[CH3:12])[OH:6]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The solution of 0.51 g of tert-butyl {1-(2-azido-1-hydroxyethyl)-3-[3-(3-methoxypropyl)-1-methyl-1H-indol-5-ylmethyl]-4-methylpentyl}carbamate in 15 ml of methanol is hydrogenated in the presence of 0.11 g of 10% Pd/C over 1 hour. The reaction mixture is clarified by filtration and concentrated by evaporation. The title compound is identified on the basis of the Rf value from the residue.
Workup
- filtrationThe reaction mixture is clarified by filtration
- concentrationconcentrated by evaporation
Sources & evidence
- ORD record
- ord-0a16c910f9be45b2bb45cf82448d5b5e
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07868036B2
Reaction notes
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