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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355247Generated: October 26, 2026

Potassium Carbonate → Methyl 1-{3-[2-[3-(phenylsulphonylamino)-phenyl]-2-hydroxy-ethylamino]-3-methyl-butyl}-1H-indole-5-carboxylate

https://huagongshe.com/reaction/2355247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium borohydrideHCID 4311764—
ReactantN-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamideHCID 57429080—
ReactantMethyl 1-(3-amino-3-methyl-butyl)-indole-5-carboxylateHCID 68453514—
CatalystTriethylamineHCID 8471—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductMethyl 1-{3-[2-[3-(phenylsulphonylamino)-phenyl]-2-hydroxy-ethylamino]-3-methyl-butyl}-1H-indole-5-carboxylateHCID 16659831—

Reaction Conditions

Temperature80 °C

Reaction Steps

154 mg (0.46 mmol) N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide (Component I) and 125 mg (0.48 mmol) methyl 1-(3-amino-3-methyl-butyl)-indole-5-carboxylate (Component IV) are dissolved in 10 ml of ethanol and combined with 4 drops of triethylamine. The reaction solution is heated to 80° C. for 17 hours. Then it is cooled to 0° C. and over a period of 2.5 hours 140 mg (3.7 mmol) sodium borohydride are added batchwise. The mixture is stirred for another hour at 0° C. and the reaction solution is then poured into a mixture of 20 ml of saturated aqueous potassium carbonate solution and 50 ml of ethyl acetate. After separation of the organic phase the aqueous phase is extracted with ethyl acetate. The combined organic phases are with washed saturated aqueous saline solution and dried on sodium sulphate. Then the solvent is eliminated in vacuo and the residue is chromatographed on silica gel (DCM/methanol=100:0:0→9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754756B2
Source datasetuspto-grants-2010_07
ORD IDord-939f452e2a78453f9dbf29b55708be13
Source noteuspto-grants-2010_07