HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[[2-[4-(Benzyloxy)-3-methoxy-phenyl]-ethyl]-(cyclopropylmethyl)amino]-N-methyl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-chloro-N-methylacetamide | HCID 66773 | — |
| Reactant | [2-(4-Benzyloxy-3-methoxy-phenyl)-ethyl]-(cyclopropylmethyl)amine | HCID 59596845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[[2-[4-(Benzyloxy)-3-methoxy-phenyl]-ethyl]-(cyclopropylmethyl)amino]-N-methyl-acetamide | HCID 25018222 | 85% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of 0.5 g (1.6 mmol) of [2-(4-benzyloxy-3-methoxy-phenyl)-ethyl]-(cyclopropylmethyl)-amine, 0.27 ml (1.92 mmol) of triethylamine, 0.207 g (1.92 mmol) of 2-chloro-N-methyl-acetamide in 4 ml of dimethylformamide was heated with microwaves to 120° C. for 2 hours. The solvent was removed under vacuum and the crude was purified by flash chromatography (ethyl acetate/hexane 0:10→9:1 gradient). 0.52 g (84% yield) of the title compound was isolated as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129427B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-0f41d43b560642c19d721bc3447e3f5f |
| Source note | uspto-grants-2012_03 |