4-Methoxybenzoic Acid → HCID 58614727, compound

HRID 922870Notes

Reaction equation

HRID 922870 reaction equation
[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1.[O:15]([C:17]1[CH:25]=[CH:24][C:20]([C:21](O)=[O:22])=[CH:19][CH:18]=1)[CH3:16]>>[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([NH:6][C:21](=[O:22])[C:20]2[CH:24]=[CH:25][C:17]([O:15][CH3:16])=[CH:18][CH:19]=2)=[CH:4][C:3]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1

Participants

3

Reactant 2

HCID 74784-Methoxybenzoic AcidHCID 401519254-Chloro-3-(pyridin-2-yl)aniline

Product 1

HCID 58614727HCID 58614727, compound

Procedure

Procedure G was used to couple 4-chloro-3-(pyridin-2-yl)aniline and 4-methoxylbenzoic acid to produce N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-methoxybenzamide. MS (Q1) 341.2 (M)+.

Sources & evidence

ORD record
ord-e5c8b728b07749038ddefbfcd523cb92
Source dataset
uspto-grants-2016_03
Patent number
US09278961B2

Reaction notes

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