HCID 18368171, compound → HCID 18368097, compound

HRID 379811Notes

Reaction equation

HRID 379811 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]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([CH3:25])[N:20]=1)=[O:18]>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]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([CH3:25])[N:20]=1)=[O:18]

Participants

3

Reactant 1

HCID 18368171HCID 18368171, compound

Product 1

HCID 18368097HCID 18368097, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

The title compound was prepared according to the procedure described in step 2 of Example 1 from 3-amino-6-chloro-1-(ethoxycarbonyl)-2-(6-methylpyridine-2-carbonyl)indole (Example 111, step 1). m.p.: 210-211° C. (ethyl acetate)

Sources & evidence

ORD record
ord-560b4202b1d54e0b9aae288af89aab14
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

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