HCID 178474770, compound → HCID 178474769, compound
Reaction equation
C([O:8][C:9]1[CH:28]=[CH:27][C:12]([O:13][C@H:14]2[CH2:19][O:18][C@@H:17]([CH2:20][CH2:21][CH2:22][NH:23][C:24](=[O:26])[CH3:25])[O:16][CH2:15]2)=[CH:11][CH:10]=1)C1C=CC=CC=1>C(O)C.[Pd]>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([O:13][C@H:14]2[CH2:15][O:16][C@@H:17]([CH2:20][CH2:21][CH2:22][NH:23][C:24](=[O:26])[CH3:25])[O:18][CH2:19]2)=[CH:27][CH:28]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
cis-N-{3-[5-(4-Benzyloxyphenoxy)-[1,3]dioxan-2-yl]propyl}acetamide (25 mg, 0.065 mmol) was dissolved in 5 ml of ethanol and hydrogenated in the presence of 0.69 mg of palladium/carbon under 3 bar for 1 h. The reaction mixture was concentrated and directly reacted further. Yield 18 mg.
Workup
- concentrationThe reaction mixture was concentrated
- customdirectly reacted further
Sources & evidence
- ORD record
- ord-725d179ca8a04b649fc752bc0661d607
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08470841B2
Reaction notes
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