4-Chloro-o-anisic acid → HCID 22493918, compound

HRID 1816588Notes

Reaction equation

HRID 1816588 reaction equation
[NH2:1][CH2:2][C:3]1[CH:4]=[C:5]([CH2:11][CH:12]([O:18][CH:19]([CH3:21])[CH3:20])[C:13]([O:15]CC)=[O:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[Cl:22][C:23]1[CH:31]=[CH:30][C:26]([C:27](O)=[O:28])=[C:25]([O:32][CH3:33])[CH:24]=1>>[Cl:22][C:23]1[CH:31]=[CH:30][C:26]([C:27]([NH:1][CH2:2][C:3]2[CH:4]=[C:5]([CH2:11][CH:12]([O:18][CH:19]([CH3:20])[CH3:21])[C:13]([OH:15])=[O:14])[CH:6]=[CH:7][C:8]=2[O:9][CH3:10])=[O:28])=[C:25]([O:32][CH3:33])[CH:24]=1

Participants

3

Reactant 2

HCID 936824-Chloro-o-anisic acidHCID 22493983Ethyl 3-[3-(aminomethyl)-4-methoxyphenyl]-2-isopropoxypropanoate

Product 1

HCID 22493918HCID 22493918, compound

Procedure

Ethyl 3-[3-(aminomethyl)-4-methoxyphenyl]-2-isopropoxypropanoate and 4-chloro-2-methoxybenzoic acid were treated in the same manners as in Example 20d) and then in Example 1d), to give 3-(3-{[(4-chloro-2-methoxybenzoyl)amino]methyl}-4-methoxyphenyl)-2-isopropoxypropanoic acid.

Sources & evidence

ORD record
ord-d7204323656f45f6b0792402a34255e2
Source dataset
uspto-grants-2005_04
Patent number
US06884821B1

Reaction notes

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