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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235087Generated: November 1, 2026

3-Chlorobenzenesulphonyl chloride → HCID 68695396, compound

https://huagongshe.com/reaction/2235087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzenesulphonyl chlorideHCID 17909—
ReactantHCID 68697366HCID 68697366—
ProductHCID 68695396HCID 68695396—

Reaction Steps

4-{[1-(3-Chloro-benzenesulfonyl)-2,3-dihydro-1H-indole-6-carbonyl]-amino}-2-fluoro-benzoic acid, m/z (ES+): 475.18 (M+H+.), was prepared in analogy to example 1, steps 1 to 5. Step 2 was performed using 4-amino-2-fluorobenzoic acid ethyl ester and yielded 2-fluoro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid ethyl ester. This was reduced to 4-[(2,3-dihydro-1H-indole-6-carbonyl)-amino]-2-fluoro-benzoic acid ethyl ester in step 3. Step 4 was performed using 3-chloro-benzenesulfonyl chloride, yielding 4-{[1-(3-chloro-benzenesulfonyl)-2,3-dihydro-1H-indole-6-carbonyl]-amino}-2-fluoro-benzoic acid ethyl ester, which was hydrolyzed in step 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713996B2
Source datasetuspto-grants-2010_05
ORD IDord-e8d5b40016214750bd6bff752f4789ba
Source noteuspto-grants-2010_05