HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → 5-(1-Diethylcarbamoyl-1-methyl-ethoxy)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 5-(1-Carboxy-1-methyl-ethoxy)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester | HCID 23393813 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(1-Diethylcarbamoyl-1-methyl-ethoxy)-2-methyl-1H-indole-3-carboxylic Acid Benzyl Ester | HCID 10159262 | 12% |
Reaction Steps
5-(1-Carboxy-1-methyl-ethoxy)-2-methyl-1H-indole-3-carboxylic acid benzyl ester (1.0 g, 2.76 mmol, 1.0 eq) was dissolved in ethylacetate (100 mL), and treated with diethylamine (0.241 g, 3.3 mmol, 1.2 eq) followed by HBTU (0.446 g, 3.3 mmol, 1.2 eq). The reaction mixture was stirred at room temperature for 24 hours and was followed by TLC (hexane/ethyl acetate 1/1). The reaction was quenched with aqueous sodium bicarbonate, extracted with ethyl acetate, and the organic layers dried over sodium sulfate, evaporated, and loaded on silica gel, followed by flash chromatography (hexane/ethyl acetate 1/1). 0.109 g of the product was obtained, 12% yield. LC/MS (ESI+) 422.52 (M+1) (C25H30N2O4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06951848B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-aec778a9fa7045b5b5bd9e8ea0a68821 |
| Source note | uspto-grants-2005_10 |