HCID 18367959, compound → HCID 18368093, compound
Reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[N:4](C(OCC)=O)[C:3]=1[C:17]([CH:19]1[CH2:24][CH2:23][CH2:22][CH:21]([CH3:25])[CH2:20]1)=[O:18]>CCCCCC.C(OCC)(=O)C>[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[NH:4][C:3]=1[C:17]([CH:19]1[CH2:24][CH2:23][CH2:22][CH:21]([CH3:25])[CH2:20]1)=[O:18]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared according to the procedure described in step 3 of Example 1 from 3-amino-6-chloro-1-ethoxycarbonyl-2-(3-methylcyclohexylcarbonyl)indole (step 2). m.p.: 140-142° C. (hexane/ethyl acetate)
Sources & evidence
- ORD record
- ord-39c1e993c38846e8b3e1104112d3e8c1
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300363B1
Reaction notes
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