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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide | HCID 57429080 | — |
| Reactant | Methyl 1-(3-amino-3-methyl-butyl)-indole-5-carboxylate | HCID 68453514 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 1-{3-[2-[3-(phenylsulphonylamino)-phenyl]-2-hydroxy-ethylamino]-3-methyl-butyl}-1H-indole-5-carboxylate | HCID 16659831 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07754756B2 |
|---|
| Source dataset | uspto-grants-2010_07 |
|---|
| ORD ID | ord-939f452e2a78453f9dbf29b55708be13 |
|---|
| Source note | uspto-grants-2010_07 |
|---|