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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715850Generated: November 2, 2026

Methyl 2-(4-aminophenyl)propionate → 2-(4-{[1-(2-Methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carbonyl]-amino}-phenyl)-propionic acid methyl ester

https://huagongshe.com/reaction/1715850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(4-aminophenyl)propionateHCID 3016109—
Reactant1-(2-Methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carboxylic acidHCID 68433807—
Product2-(4-{[1-(2-Methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carbonyl]-amino}-phenyl)-propionic acid methyl esterHCID 68511855—

Reaction Steps

1-(2-Methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carboxylic acid was converted to the title compound in analogy to example 8, steps 3 and 4. Step 3 was performed using 2-(4-amino-phenyl)-propionic acid methyl ester and 1-(2-methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carboxylic acid and yielded 2-(4-{[1-(2-methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carbonyl]-amino}-phenyl)-propionic acid methyl ester, which was hydrolyzed to 2-(4-{[1-(2-methoxy-5-methyl-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline-7-carbonyl]-amino}-phenyl)-propionic acid in step 4, MS (ISP): m/e=526.2 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799933B2
Source datasetuspto-grants-2010_09
ORD IDord-5c128c36b99841358a23ee4b0d3ae7dc
Source noteuspto-grants-2010_09