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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241141Generated: November 2, 2026

3-(Trifluoromethyl)benzenesulfonyl chloride → 2-Methoxy-4-[3-(3-trifluoromethyl-benzenesulfonylamino)-benzoylamino]-benzoic acid ethyl ester

https://huagongshe.com/reaction/2241141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
Reactant4-(3-Amino-benzoylamino)-2-methoxy-benzoic acid ethyl esterHCID 68407880—
Product2-Methoxy-4-[3-(3-trifluoromethyl-benzenesulfonylamino)-benzoylamino]-benzoic acid ethyl esterHCID 68406228—

Reaction Steps

2-Methoxy-4-[3-(3-trifluoromethyl-benzenesulfonylamino)-benzoylamino]-benzoic acid, MS (ISP): m/e=493.3 (M−H), was prepared in analogy to example 1, steps A to D. Step A was performed using 4-amino-2-methoxy-benzoic acid ethyl ester and yielded 2-methoxy-4-(3-nitro-benzoylamino)-benzoic acid ethyl ester. This was reduced to 4-(3-amino-benzoylamino)-2-methoxy-benzoic acid ethyl ester in step B. This was coupled with 3-trifluoromethyl-benzenesulfonyl chloride in step C, yielding 2-methoxy-4-[3-(3-trifluoromethyl-benzenesulfonylamino)-benzoylamino]-benzoic acid ethyl ester, which was hydrolyzed in step D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723538B2
Source datasetuspto-grants-2010_05
ORD IDord-96a6d8ced006489098147beb6ea44f0a
Source noteuspto-grants-2010_05