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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627227Generated: October 30, 2026

Diisopropylethylamine → (2S,5R)-6-(allyloxy)-3-ethyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-ene-2-carboxamide

https://huagongshe.com/reaction/627227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactant(R)-5-(allyloxyamino)-3-ethyl-1,2,5,6-tetrahydropyridine-2-carboxamideHCID 89852076—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(2S,5R)-6-(allyloxy)-3-ethyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-ene-2-carboxamideHCID 89851798255.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (R)-5-(allyloxyamino)-3-ethyl-1,2,5,6-tetrahydropyridine-2-carboxamide (Intermediate 214, 0.35 g, 1.55 mmol) and diisopropylethyl amine (1.082 mL, 6.21 mmol) in acetonitrile (110 mL) at 0° C. was added triphosgene (0.157 g, 0.53 mmol) as a solution in acetonitrile (4 mL). The triphosgene solution was added at a rate of 4 mL/hour. Once addition was complete the reaction was stirred at 0° C. for ˜1 hour. The reaction mixture was diluted with ethyl acetate, then washed with saturated sodium bicarbonate and brine. The aqueous washes were extracted once with dichloromethane. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (0%-100% ethyl acetate/hexanes) afforded the title compound (0.340 g, 87%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309245B2
Source datasetuspto-grants-2016_04
ORD IDord-ff572deaaf354ddc96446791725c2236
Source noteuspto-grants-2016_04