Ethyl 6-hydroxy-7-(prop-2-en-1-yl)-1H-indole-2-carboxylate → HCID 20183534, compound
Reaction equation
[OH:1][C:2]1[C:10]([CH2:11][CH:12]=[CH2:13])=[C:9]2[C:5]([CH:6]=[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[NH:8]2)=[CH:4][CH:3]=1>C(O)C.[Pd]>[OH:1][C:2]1[C:10]([CH2:11][CH2:12][CH3:13])=[C:9]2[C:5]([CH:6]=[C:7]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[NH:8]2)=[CH:4][CH:3]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The product of step b) was dissolved in dry ethanol (350 ml), treated with 10% Pd/C (0.3 g) and hydrogenated at 35 psi at room temperature until H2 uptake ceased (1.5 hours). The catalyst was filtered off and the filtrate evaporated to dryness.
Workup
- custom(1.5 hours)
- filtrationThe catalyst was filtered off
- customthe filtrate evaporated to dryness
Sources & evidence
- ORD record
- ord-15372c7080454dc689a6f0ecb4b3b457
- Source dataset
- uspto-grants-1987_10
- Patent number
- US04698345
Reaction notes
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