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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656742Generated: October 30, 2026

4-Chlorobenzoyl chloride → HCID 58372843, compound

https://huagongshe.com/reaction/656742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantHCID 58372835HCID 58372835—
ProductHCID 58372843HCID 58372843—

Reaction Steps

As described for Example 10, [3-(2-bromomethyl-4-nitro-phenoxy)-4-methoxy-phenyl]-acetic acid ethyl ester and 5-methyl-1,3,4-thiadiazole-2-thiol were reacted to form {4-methoxy-3-[2-(5-methyl-[1,3,4]thiadiazol-2-ylsulfanylmethyl)-4-nitro-phenoxy]-phenyl}-acetic acid ethyl ester, which was reduced to {3-[4-amino-2-(5-methyl-[1,3,4]thiadiazol-2-ylsulfanylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester and then treated with 4-chlorobenzoyl chloride to provide {3-[4-(4-chloro-benzoylamino)-2-(5-methyl-[1,3,4]thiadiazol-2-ylsulfanylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester. Hydrolysis of the ester to the acid provided Compound 19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071807B2
Source datasetuspto-grants-2011_12
ORD IDord-b55fe7847a7d425b876915c9f22757f7
Source noteuspto-grants-2011_12