Ethyl 2-(4-methoxy-2-nitroanilino)benzo[b]thiophene-3-carboxylate → Ethyl 2-(2-amino-4-methoxy-anilino)benzo[b]thiophene-3-carboxylate

HRID 649914Notes

Reaction equation

HRID 649914 reaction equation
[CH3:1][O:2][C:3]1[CH:23]=[CH:22][C:6]([NH:7][C:8]2[S:12][C:11]3[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=3[C:9]=2[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[C:5]([N+:24]([O-])=O)[CH:4]=1.[H][H]>[C].[Pd].C(OCC)(=O)C>[NH2:24][C:5]1[CH:4]=[C:3]([O:2][CH3:1])[CH:23]=[CH:22][C:6]=1[NH:7][C:8]1[S:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[C:9]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18]

Participants

5

Reactant 2

HCID 18422251Ethyl 2-(4-methoxy-2-nitroanilino)benzo[b]thiophene-3-carboxylateHCID 178418361HCID 178418361, compound

Product 1

HCID 18422191Ethyl 2-(2-amino-4-methoxy-anilino)benzo[b]thiophene-3-carboxylate

Reagents, catalysts & solvents 2

HCID 178418390HCID 178418390, compoundCatalystHCID 8857Ethyl AcetateSolvent

Procedure

In the same manner as in Starting Material Synthesis Example 19 and using ethyl 2-(4-methoxy-2-nitroanilino)benzo[b]thiophene-3-carboxylate, ethyl acetate, 10% palladium-carbon and hydrogen (60 atm kg/cm2), ethyl 2-(2-amino-4-methoxyanilino)benzo[b]thiophene-3-carboxylate is obtained.

Workup

  1. customMaterial Synthesis Example 19

Sources & evidence

ORD record
ord-1537b3ebf8ea4a18a9b4c7ce0530d382
Source dataset
uspto-grants-2001_08
Patent number
US06271225B1

Reaction notes

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