HCID 18367895, compound → 3-Amino-6-chloro-2-(4-methoxy-pyridine-2-carbonyl)indole

HRID 379771Notes

Reaction equation

HRID 379771 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]=[C:23]([O:25][CH3:26])[CH:22]=[CH:21][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]=[C:23]([O:25][CH3:26])[CH:22]=[CH:21][N:20]=1)=[O:18]

Participants

3

Reactant 1

HCID 18367895HCID 18367895, compound

Product 1

HCID 183680323-Amino-6-chloro-2-(4-methoxy-pyridine-2-carbonyl)indole

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

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-(4-methoxypyridine-2-carbonyl)indole (step 1). m.p.: 195-196° C. (ethyl acetate)

Sources & evidence

ORD record
ord-b2f5b8d934ef4469b462f8831008f1d0
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

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