5-Chlorosalicylic Acid → HCID 17860203, compound

HRID 421145Notes

Reaction equation

HRID 421145 reaction equation
[Cl:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=O)[C:5]([OH:11])=[CH:4][CH:3]=1.[NH2:12][C:13]1[CH:14]=[C:15]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:11])=[C:6]([CH:10]=1)[C:7]([NH:12][C:13]1[CH:14]=[C:15]([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20])=[O:9]

Participants

3

Reactant 2

HCID 94475-Chlorosalicylic AcidHCID 1234895-Phenyl-o-anisidine

Product 1

HCID 17860203HCID 17860203, compoundYield 37%

Procedure

Using 5-chlorosalicylic acid and 3-amino-4-methoxybiphenyl as the raw materials, the same operation as the example 16 gave the title compound.

Sources & evidence

ORD record
ord-bd64f4a7afc34b4b93c8176d9d8c6eca
Source dataset
uspto-grants-2012_01
Patent number
US08097759B2

Reaction notes

Loading…