HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → (5-Ethylcarbamoyl-[1,3,4]oxadiazol-2-ylmethyl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Ethyl 5-(((tert-butoxycarbonyl)amino)methyl)-1,3,4-oxadiazole-2-carboxylate | HCID 10084542 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Ethylcarbamoyl-[1,3,4]oxadiazol-2-ylmethyl)-carbamic acid tert-butyl ester | HCID 57940543 | — |
Reaction Steps
To a solution of 5-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]-1,3,4-oxadiazole-2-carboxylic acid ethyl ester (prepared as described in JOC (1995), 60(10), 3112-20) (0.150 g) in methanol (5 ml) was added a solution of 2.0M ethylamine in tetrahydrofuran (3 ml). The solution was left standing at 20° C. for 1.5 h. The solvent was removed by evaporation using a stream of nitrogen to give the title compound as a yellow gum (0.139 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07622464B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-fb04399e7fe94316a35a10490250308a |
| Source note | uspto-grants-2009_11 |