HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → [5-Oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 5-Oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)pyrrolidin-3-carboxylic acid | HCID 86724924 | — |
| Product | [5-Oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester | HCID 86724925 | 61% |
Reaction Steps
A mixture of 5-oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)pyrrolidin-3-carboxylic acid (300 mg, 1.09 mmol), diphenyl phosphoryl azide (351 μl, 1.63 mmol), triethylamine (380 μl, 2.73 mmol) and tert-butyl alcohol (10 ml) was heated under reflux for 24 hours. The reaction solution was cooled, the solvent was then removed under reduced pressure, and the obtained residue was suspended in ethyl acetate to collect the insoluble material by filtration. The obtained residue was purified by silica gel column chromatography (chloroform/methanol) to yield 230 mg (61%) of the title compound in the form of a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952010B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-c95225bd4b8642a38dc0a195e473730c |
| Source note | uspto-grants-2015_02 |