HCID 18368017, compound → HCID 18367785, compound

HRID 379745Notes

Reaction equation

HRID 379745 reaction equation
[C:1]([NH:4][C:5]1[C:13]2[C:8](=[CH:9][C:10]([Cl:14])=[CH:11][CH:12]=2)[N:7](C(OCC)=O)[C:6]=1[C:20](=[O:28])[C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[CH:22]=1)(=[O:3])[CH3:2]>C(O)C>[C:1]([NH:4][C:5]1[C:13]2[C:8](=[CH:9][C:10]([Cl:14])=[CH:11][CH:12]=2)[NH:7][C:6]=1[C:20](=[O:28])[C:21]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[CH:22]=1)(=[O:3])[CH3:2]

Participants

3

Reactant 1

HCID 18368017HCID 18368017, compound

Product 1

HCID 18367785HCID 18367785, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The title compound was prepared according to the procedure described in step 2 of Example 2 (Method A) from 3-acetylamino-6-chloro-2-(3-fluorobenzoyl)-1-(ethoxycarbonyl)indole (step 1). m.p.: 201-202° C. (ethanol)

Sources & evidence

ORD record
ord-5301c72639f142e78c516fa910ab8f73
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

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