HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 19838218, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Aminoindan hydrochloride | HCID 122764 | — |
| Reactant | 6-{[2-(3,4-Dimethoxyphenyl)ethyl]amino}-6-oxohexanoic acid | HCID 13935767 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19838218 | HCID 19838218 | 79.3% |
Reaction Steps
6-[2-(3,4-Dimethoxyphenyl)ethylamino]-6-oxohexanoic acid (6.0 g, 0.019 mole) was dissolved in dry dichloromethane (200 ml) and triethylamine (2.28 g, 0.021 mole) added followed by ethyl chloroformate (1.86 ml, 0.019 mole) at 0°. The solution was stirred at 0° for 30 min and a solution of 2-aminoindane hydrochloride (3.3 g, 0.019 mole) and triethylamine (2.52 ml 0.019) in dry dichloromethane (200 ml) added, allowed to warm to room temperature and stirred for a further 18 hr. The reaction mixture was washed with water, dried (MgSO4) and evaporated and the residue recrystallised from methanol to give the sub-title compound as a white solid (6.4 g), mp 162°-4°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04885313 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-cd6163c5faa9473a93dbe13b26dae5ba |
| Source note | uspto-grants-1989_12 |