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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713751Generated: October 26, 2026

Triethylamine → Methyl 4-{2-[(benzofuran-2-yl-carbonyl)amino]ethylsulfanyl}benzoate

https://huagongshe.com/reaction/713751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzofuran-2-carboxylic acidHCID 10331—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantMethyl 4-(2-aminoethylsulfanyl)benzoate hydrochlorideHCID 66687893—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-{2-[(benzofuran-2-yl-carbonyl)amino]ethylsulfanyl}benzoateHCID 6668794638.8%

Reaction Steps

Methyl 4-(2-aminoethylsulfanyl)benzoate hydrochloride (0.248 g, 1.00 mmol), was combined with benzofuran-2-carboxylic acid (0.162 g, 1.00 mmol) and HBTU (0.379 g, 1.00 mmol) in DMF (5 ml) at room temperature. Triethylamine (0.307 ml, 2.2 mmol) was added and the reaction mixture was stirred at room temperature overnight. Saturated aqueous NaHCO3 (15 ml) was added to give precipitates which was broken up by the addition of water (20 ml). The solid was filtered and the cake was dissolved in ethyl acetate. The residual water was removed by pipette and hexane was added to give methyl 4-{2-[(benzofuran-2-ylcarbonyl)-amino]ethylsulfanyl}benzoate (0.138 g) as a gum which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186347B1
Source datasetuspto-grants-2015_11
ORD IDord-9cc4dc6003e84a6fbfd96f54578736d3
Source noteuspto-grants-2015_11