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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495602Generated: October 25, 2026

(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanone → 3-{4-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl}-propionic acid methyl ester

https://huagongshe.com/reaction/495602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)methanoneHCID 22327305—
ReactantMethyl 3-[4-(chlorosulfonyl)phenyl]propanoateHCID 23158517—
Product3-{4-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenylsulfamoyl]-phenyl}-propionic acid methyl esterHCID 10322607—

Reaction Steps

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using (2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-3-yl)-methanone and 3-(4-Chlorosulfonyl-phenyl)-propionic acid methyl ester and purified by HPLC. 1H NMR (CDCl3) δ 9.66 (br s, 1H, NH), 8.34 (d, 1H, J=2.2 Hz), 7.75 (d, 1H, J=8.8 Hz), 7.72 (d, 1H, J=8.0 Hz, J=2.2 Hz), 7.56 (d, 2H, J=8.4 Hz), 7.51 (dd, 1H, J=8.8 Hz, J=2.2 Hz), 7.32 (d 1H, J=2.2 Hz), 7.26 (d, 1H, J=7 Hz), 7.09 (d, 2H, J=8.4 Hz), 3.65 (s, 3H), 2.97 (t, 2H, J=7.6 Hz), 2.66 (s, 3H), 2.51 (t, 2H, J=7.6 Hz). MS: m/z 473 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939885B2
Source datasetuspto-grants-2005_09
ORD IDord-7d1524e441994a2fb690a3a65ad57ab8
Source noteuspto-grants-2005_09