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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750246Generated: November 1, 2026

Hydrochloric Acid → 4-(2-Methyl-cyclopentylamino)-3-(2-thiophen-2-yl-acetylamino)-benzoic acid methyl ester

https://huagongshe.com/reaction/1750246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant3-Amino-4-(2-methyl-cyclopentylamino)-benzoic acid methyl esterHCID 63279519—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Solvent2,4,6-Tris((dimethylamino)methyl)phenolHCID 7026—
SolventEthyl AcetateHCID 8857—
Product4-(2-Methyl-cyclopentylamino)-3-(2-thiophen-2-yl-acetylamino)-benzoic acid methyl esterHCID 86714453100.3%

Reaction Steps

To a solution of 3.44 g of thiophen-2-yl-acetic acid in 40 ml of dry DMF 3.62 g of HOAT, 6.48 g of EDC and 12 ml of DIPEA were added at 0° C. After 30 min 6.00 g of 3-Amino-4-(2-methyl-cyclopentylamino)-benzoic acid methyl ester were added, and the reaction was stirred at rt for 16 h. The reaction was then poured into water and the pH was adjusted to 3 by the addition of 2 m aqueous hydrochloric acid. Ethyl acetate was added and the layers were separated. The aqueous layer was extracted with ethyl acetate three times. The combined organic phases were washed with saturated aqueous sodium bicarbonate solution and brine, dried over magnesium sulphate and concentrated to obtain 9.03 g (100%) of 4-(2-Methyl-cyclopentylamino)-3-(2-thiophen-2-yl-acetylamino)-benzoic acid methyl ester, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156796B2
Source datasetuspto-grants-2015_10
ORD IDord-1b185dc523244d1fb0e5e008317041e5
Source noteuspto-grants-2015_10