5-(Trifluoromethyl)-m-anisidine → HCID 59265134, compound

HRID 558370Notes

Reaction equation

HRID 558370 reaction equation
[CH3:1][O:2][C:3]1[C:8]([C:9]([OH:11])=O)=[CH:7][C:6]([C:12]([NH2:14])=[O:13])=[CH:5][CH:4]=1.[CH3:15][O:16][C:17]1[CH:18]=[C:19]([CH:21]=[C:22]([C:24]([F:27])([F:26])[F:25])[CH:23]=1)[NH2:20]>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:12]([NH2:14])=[O:13])=[CH:7][C:8]=1[C:9]([NH:20][C:19]1[CH:21]=[C:22]([C:24]([F:26])([F:27])[F:25])[CH:23]=[C:17]([O:16][CH3:15])[CH:18]=1)=[O:11]

Participants

3

Reactant 2

HCID 6056715-(Trifluoromethyl)-m-anisidineHCID 132228085-Carbamoyl-2-methoxybenzoic acid

Product 1

HCID 59265134HCID 59265134, compound

Procedure

The captioned compound was synthesized from 6-methoxyisophthalamic acid and 3-methoxy-5-trifluoromethylaniline by the same procedure as in the manufacturing method described in step C of Example 1-3-1.

Sources & evidence

ORD record
ord-2e56e77043b64562aac5f78853d138e1
Source dataset
uspto-grants-2011_11
Patent number
US08063046B2

Reaction notes

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