Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 9868116 | HCID 9868116 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 91293352 | HCID 91293352 | — |
Reaction Steps
1.5 g (3.37 mmol) of phenylmethyl [2-chloro-4-(5-oxo-4-(pyrrolidin-3-yl)-4,5-dihydro-1,3,4-oxadiazol-2-yl)-5-methoxyphenyl]carbamate dissolved in 26 ml of acetonitrile, and 1.41 ml (10.1 mmol) of triethylamine are placed in a 100 ml three-necked round-bottomed flask. A solution of 0.6 g (4.38 mmol) of 1-bromobutane in 4 ml of acetonitrile is added and the mixture is heated at 60° C. for 15 h.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248757B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-e84f6cc1cd9c4fd48323cd13b0de8075 |
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| Source note | uspto-grants-2001_06 |
|---|