3-Acetylamino-2-benzoyl-5-chloro-1-(ethoxycarbonyl)indole → 3-Acetylamino-2-benzoyl-5-chloroindole

HRID 379796Notes

Reaction equation

HRID 379796 reaction equation
[C:1]([NH:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([Cl:14])[CH:12]=2)[N:7](C(OCC)=O)[C:6]=1[C:20](=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)(=[O:3])[CH3:2]>C(OCC)(=O)C>[C:1]([NH:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([Cl:14])[CH:12]=2)[NH:7][C:6]=1[C:20](=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)(=[O:3])[CH3:2]

Participants

3

Reactant 1

HCID 183677233-Acetylamino-2-benzoyl-5-chloro-1-(ethoxycarbonyl)indole

Product 1

HCID 183680793-Acetylamino-2-benzoyl-5-chloroindole

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

The title compound was prepared according to the procedure described in step 2 of Example 2 (Method A) and from 3-acetylamino-2-benzoyl-5-chloro-1-(ethoxycarbonyl)indole (step 2). m.p.: 200-201° C. (ethyl acetate)

Sources & evidence

ORD record
ord-d1630cd1aef04d1daa6b4f79c3bdab50
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

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