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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173808Generated: October 27, 2026

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

https://huagongshe.com/reaction/1173808

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-yl-carbonyl)-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 numberUS07834054B2
Source datasetuspto-grants-2010_11
ORD IDord-c6dbdd8e88f1469bacbed526e04a88c7
Source noteuspto-grants-2010_11