HCID 67517747, compound → HCID 86665533, compound
Reaction equation
[C:1]([O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][S:14]([CH2:17][CH2:18][C:19]([NH:22]C(=O)OCC1C=CC=CC=1)([CH3:21])[CH3:20])(=[O:16])=[O:15])([CH3:4])([CH3:3])[CH3:2]>CO.[Pd]>[C:1]([O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][S:14]([CH2:17][CH2:18][C:19]([CH3:21])([NH2:22])[CH3:20])(=[O:16])=[O:15])([CH3:4])([CH3:3])[CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of benzyl 4-(2-(2-(2-tert-butoxyethoxy)ethoxy)ethylsulfonyl)-2-methylbutan-2-ylcarbamate (79.5 mg, 0.168 mmol) in MeOH (2 ml) was put under a N2 atmosphere and 10% Pd/C (30 mg) was added. A H2 atmosphere (1.3 atm) was added, and the slurry stirred for 2 h. The suspension was filtered (0.45 um PTFE) and the solution concentrated in vacuo. The residue was used without further purification. LRMS (ESI/APCI): 340 [M+H]+.
Workup
- additionA H2 atmosphere (1.3 atm) was added
- filtrationThe suspension was filtered (0.45 um PTFE)
- concentrationthe solution concentrated in vacuo
- customThe residue was used without further purification
Sources & evidence
- ORD record
- ord-93869485c1b841aabfd6275830f88daa
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09248117B2
Reaction notes
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