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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015638Generated: October 26, 2026

Cesium carbonate → 3-Cyclopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1015638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantCyclopropylamineHCID 69828—
ReactantBinap, (A+-)-HCID 634876—
ReactantMethyl 3-bromo-5-phenyl-thiophene-2-carboxylateHCID 20775762—
SolventTolueneHCID 1140—
Product3-Cyclopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 2077576422%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 3-Bromo-5-phenyl-thiophene-2-carboxylic acid methyl ester (250 mg, 0.89 mmol) in toluene (25 ml) was added cyclopropylamine (57 mg, 1.0 mmol), cesium carbonate (382 mg, 1.2 mmol), BINAP (50 mg, 0.08 mmol) and tris (dibenzyli-denacetone)dipaladium (0) (38 mg, 0.04 mmol). The reaction mixture was stirred for 16 h at 110° C. in a sealed tube. The mixture was partitioned between toluene (20 mL) and water (20 mL) and the organic layer was separated. The aqueous phase was washed twice with toluene (2×10 mL) and the combined toluene layer was dried (MgSO4), concentrated and the residue was purified by preparative chromatography (10% EtOAc/Hexane) to obtain 52 mg (22%) of 3-Cyclopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester. NMR 1H (CDCl3, 400 MHz): 7.67-7.62 ppm (m, 2H, Haro); 7.43-7.32 ppm (m, 3H, Haro); 7.16 ppm (s, 1H, Haro); 3.82 ppm (S, 3H); 2.65 ppm (m, 1H); 0.62 ppm (m, 2H); 0.35 ppm (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-78c2b097b9ca481783350ce25cc76f74
Source noteuspto-grants-2011_07