HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Methoxycarbonylethylcarbonyloxy-1-phenylindole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-[3-(N,N-diethylamino)-2-hydroxypropylaminocarbonyl]-3-hydroxy-1-phenylindole hydrochloride | HCID 54724113 | — |
| Reactant | Succinic acid methylester chloride | HCID 86605420 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methoxycarbonylethylcarbonyloxy-1-phenylindole hydrochloride | HCID 86742821 | — |
Reaction Steps
2.1 g of 2-[3-(N,N-diethylamino)-2-hydroxypropylaminocarbonyl]-3-hydroxy-1-phenylindole hydrochloride (0.005 mole) are mixed in 25 ml of methylene chloride with 0.7 ml triethylamine (0.005 mole) and 0.6 ml of succinic acid methylester chloride and the reaction mixture agitated for 1 h at room temperature. The solution is then washed with a saturated solution of sodium chloride, dried over sodium sulfate, filtered and evaporated. The residue is purified by low pressure chromatography using methylene chloride as the elution agent, as described in Example 3. 2-[3-N,N-diethylamino)-2-hydroxypropylaminocarbonyl]-3-methoxycarbonylethylcarbonyloxy-1-phenylindole hydrochloride is obtained as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04814345 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-d81c6409718e4dbbaa0a27e706b50e8a |
| Source note | uspto-grants-1989_03 |