Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 9818855 | HCID 9818855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53643946 | HCID 53643946 | 60.6% |
Reaction Steps
To a suspension of 6,7-dimethoxy-1-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinolin-8-ol (103 mg, 0.312 mmole) in dichloromethane (2 ml) were added N,N-dimethylglysine hydrochloride (52.2 mg, 0.374 mole) and HOBt (57.3 mg, 0.374 mmole) at room temperature under nitrogen. Then triethylamine (56.5 μl, 0.405 mmole) and EDCI (71.7 mg, 0.374 mmole) were added to the mixture at 0° C. The reaction mixture was stirred at 0° C. for 1.5 hours and at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure, and water was added to the residue. The mixture was extracted with chloroform. The combined extracts were successively washed with a saturated aqueous sodium hydrogencarbonate solution and brine, dried over MgSO4, and concentrated under reduced pressure. The residue was recrystallized from methanol to give the desired compound (78.4 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05362736 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-0fdbb02e165d4ae78f99e79dcdf067af |
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| Source note | uspto-grants-1994_11 |
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