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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846993Generated: October 31, 2026

tert-Butanol → [5-Oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1846993

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-Oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)pyrrolidin-3-carboxylic acidHCID 86724924—
Product[5-Oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)pyrrolidin-3-yl]carbamic acid tert-butyl esterHCID 8672492561%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952010B2
Source datasetuspto-grants-2015_02
ORD IDord-c95225bd4b8642a38dc0a195e473730c
Source noteuspto-grants-2015_02